NEMUS Bioscience is developing cannabinoid-based therapies using compounds licensed from the University of Mississippi, the only federally-approved source of cannabis in the US. Their lead compound NB1111 is a THC prodrug for glaucoma entering preclinical studies. In addition to ophthalmic targets, NEMUS' pipeline includes programs for MS, anxiety, epilepsy, and MRSA, with various delivery methods including topical ocular, buccal patch, and suppository. The company partners with thought leaders in ophthalmology and cannabinoid science to advance its portfolio of near-term and longer-term projects targeting unmet medical needs.
NEMUS Bioscience is developing cannabinoid-based therapies for diseases including glaucoma, chemotherapy-induced nausea and vomiting (CINV), and chemotherapy-induced peripheral neuropathy (CIPN). Their lead product candidates include NB1111, a THC prodrug for glaucoma, and NB1222, a THC prodrug suppository for CINV. NEMUS has exclusive rights to cannabinoid compounds and formulations from the University of Mississippi, the only federally-approved source of cannabis compounds in the US. They are developing these prodrugs to improve bioavailability and provide more predictable delivery compared to existing oral cannabinoid therapies.
NEMUS Bioscience is a publicly traded biotech company focused on developing cannabinoid-based therapies. The document discusses NEMUS' drug development pipeline including NB1222 for chemotherapy-induced nausea and vomiting (CINV), NB1111 for glaucoma, and research on CBD derivatives for chemotherapy-induced peripheral neuropathy (CIPN) and methicillin-resistant Staphylococcus aureus (MRSA). The document provides market data and potential advantages of NEMUS' prodrug formulations which are designed to improve cannabinoid delivery and avoid first-pass liver metabolism.
Nemus Bioscience had a productive year, advancing multiple drug candidates in oncology supportive care, ophthalmology, and anti-infectives. Key achievements included licensing CBD derivatives from the University of Mississippi, completing preclinical studies, and establishing partnerships for drug development and manufacturing. Looking forward, Nemus aims to maintain financing, advance formulations, form strategic partnerships, qualify for grants, and increase awareness to support its pipeline of cannabinoid-based therapies. The main challenges will be securing adequate capital and establishing partnerships to fund development in a non-dilutive manner.
Nemus Bioscience Inc. Investor Presentation (062915)NemusBioscience
NEMUS Bioscience is developing cannabinoid-based pharmaceuticals to treat unmet medical needs. It has licensed intellectual property from the University of Mississippi related to novel delivery methods and compositions of cannabinoids. Its lead product NB1111 is a proprietary formulation of a THC prodrug being developed as a topical treatment for glaucoma, with the potential to be the first medication to target the optic nerve through multiple mechanisms in addition to lowering intraocular pressure. NEMUS is seeking funding to complete IND-enabling studies and a Phase 1b/2a clinical trial for NB1111 in glaucoma patients.
This document provides an overview of NEMUS Bioscience, a biotech company focused on developing cannabinoid-based therapies. It discusses NEMUS' partnership with the University of Mississippi, its product pipeline including treatments for glaucoma, chemotherapy side effects, and antibiotic-resistant infections, and provides highlights of recent milestones such as positive studies of a drug for glaucoma and the identification of a molecule for chemotherapy-induced neuropathy. The document also gives financial information about NEMUS and states that it is advancing therapies in large potential markets through proprietary cannabinoid molecules.
This document provides an overview of NEMUS Bioscience, a publicly traded life sciences company focused on developing cannabinoid-based therapies. Some key points:
- NEMUS has exclusive partnerships with the University of Mississippi, the only entity licensed to study cannabinoids, giving it access to 48 years of research.
- It has a pipeline of drug candidates targeting large markets like glaucoma, chemotherapy side effects, and pain, in preclinical and research stages.
- Target indications include ocular diseases, anti-infectives for bacteria/viruses, and pain syndromes.
- Recent milestones include in-licensing a CBD derivative from UM to research chemotherapy induced
- Palisade Bio was formed through the merger of Leading BioSciences and Seneca to focus on developing drugs to restore intestinal barrier health.
- Their lead product, LB1148, is an oral protease inhibitor that has shown in clinical trials to accelerate the return of normal bowel function after surgery by 30%.
- They plan to initiate a Phase 3 trial in 2021 to evaluate LB1148 in improving GI recovery in neonates undergoing cardiac surgery, which could potentially qualify for priority review.
- If successful, LB1148 has the potential to reduce postoperative complications and lower healthcare costs through shorter hospital stays.
Bellus health agm presentation en finalBellusHealth
- The document summarizes an annual general meeting for shareholders of BELLUS Health Inc. held on May 15, 2018.
- BELLUS is developing BLU-5937, a potentially best-in-class drug for chronic cough that selectively targets P2X3 receptors. Chronic cough affects millions of people and current treatments have significant side effects.
- BLU-5937 has shown potential to be as effective as the leading P2X3 drug in development (MK-7264) at reducing cough frequency without impacting taste, which MK-7264 does. BLU-5937 is expected to have twice daily oral dosing.
NEMUS Bioscience is developing cannabinoid-based therapies for diseases including glaucoma, chemotherapy-induced nausea and vomiting (CINV), and chemotherapy-induced peripheral neuropathy (CIPN). Their lead product candidates include NB1111, a THC prodrug for glaucoma, and NB1222, a THC prodrug suppository for CINV. NEMUS has exclusive rights to cannabinoid compounds and formulations from the University of Mississippi, the only federally-approved source of cannabis compounds in the US. They are developing these prodrugs to improve bioavailability and provide more predictable delivery compared to existing oral cannabinoid therapies.
NEMUS Bioscience is a publicly traded biotech company focused on developing cannabinoid-based therapies. The document discusses NEMUS' drug development pipeline including NB1222 for chemotherapy-induced nausea and vomiting (CINV), NB1111 for glaucoma, and research on CBD derivatives for chemotherapy-induced peripheral neuropathy (CIPN) and methicillin-resistant Staphylococcus aureus (MRSA). The document provides market data and potential advantages of NEMUS' prodrug formulations which are designed to improve cannabinoid delivery and avoid first-pass liver metabolism.
Nemus Bioscience had a productive year, advancing multiple drug candidates in oncology supportive care, ophthalmology, and anti-infectives. Key achievements included licensing CBD derivatives from the University of Mississippi, completing preclinical studies, and establishing partnerships for drug development and manufacturing. Looking forward, Nemus aims to maintain financing, advance formulations, form strategic partnerships, qualify for grants, and increase awareness to support its pipeline of cannabinoid-based therapies. The main challenges will be securing adequate capital and establishing partnerships to fund development in a non-dilutive manner.
Nemus Bioscience Inc. Investor Presentation (062915)NemusBioscience
NEMUS Bioscience is developing cannabinoid-based pharmaceuticals to treat unmet medical needs. It has licensed intellectual property from the University of Mississippi related to novel delivery methods and compositions of cannabinoids. Its lead product NB1111 is a proprietary formulation of a THC prodrug being developed as a topical treatment for glaucoma, with the potential to be the first medication to target the optic nerve through multiple mechanisms in addition to lowering intraocular pressure. NEMUS is seeking funding to complete IND-enabling studies and a Phase 1b/2a clinical trial for NB1111 in glaucoma patients.
This document provides an overview of NEMUS Bioscience, a biotech company focused on developing cannabinoid-based therapies. It discusses NEMUS' partnership with the University of Mississippi, its product pipeline including treatments for glaucoma, chemotherapy side effects, and antibiotic-resistant infections, and provides highlights of recent milestones such as positive studies of a drug for glaucoma and the identification of a molecule for chemotherapy-induced neuropathy. The document also gives financial information about NEMUS and states that it is advancing therapies in large potential markets through proprietary cannabinoid molecules.
This document provides an overview of NEMUS Bioscience, a publicly traded life sciences company focused on developing cannabinoid-based therapies. Some key points:
- NEMUS has exclusive partnerships with the University of Mississippi, the only entity licensed to study cannabinoids, giving it access to 48 years of research.
- It has a pipeline of drug candidates targeting large markets like glaucoma, chemotherapy side effects, and pain, in preclinical and research stages.
- Target indications include ocular diseases, anti-infectives for bacteria/viruses, and pain syndromes.
- Recent milestones include in-licensing a CBD derivative from UM to research chemotherapy induced
- Palisade Bio was formed through the merger of Leading BioSciences and Seneca to focus on developing drugs to restore intestinal barrier health.
- Their lead product, LB1148, is an oral protease inhibitor that has shown in clinical trials to accelerate the return of normal bowel function after surgery by 30%.
- They plan to initiate a Phase 3 trial in 2021 to evaluate LB1148 in improving GI recovery in neonates undergoing cardiac surgery, which could potentially qualify for priority review.
- If successful, LB1148 has the potential to reduce postoperative complications and lower healthcare costs through shorter hospital stays.
Bellus health agm presentation en finalBellusHealth
- The document summarizes an annual general meeting for shareholders of BELLUS Health Inc. held on May 15, 2018.
- BELLUS is developing BLU-5937, a potentially best-in-class drug for chronic cough that selectively targets P2X3 receptors. Chronic cough affects millions of people and current treatments have significant side effects.
- BLU-5937 has shown potential to be as effective as the leading P2X3 drug in development (MK-7264) at reducing cough frequency without impacting taste, which MK-7264 does. BLU-5937 is expected to have twice daily oral dosing.
The document discusses the benefits of exercise for mental health. Regular physical activity can help reduce anxiety and depression and improve mood and cognitive functioning. Exercise causes chemical changes in the brain that may help boost feelings of calmness and well-being.
Daniel Sheline completed a co-op term at Toyota Technical Center from January to May 2007. During this term, he supported the ED2 470L vehicle design team and worked on several projects. He improved his CATIA and engineering design skills, learned Toyota's product development process, and strengthened his desire to have a career in automotive design.
The Next Million
ESA Earth Observation Summer School
Frascati (Rome), Italy
August 8, 2016
Summary: how can we get more people involved applying technical and research skills to tackle the SDGs. Includes extensive notes.
https://earth.esa.int/web/eo-summer-school/home1
Aspendos was an ancient Greek city founded around 1000 BC in Asia Minor that grew wealthy through trade. In the 5th century BC it became the most important city in the region of Pamphylia. It surrendered to the Roman Empire in 190 BC, after which the Romans pillaged its artistic treasures. The theater was built in 155 AD by the Greek architect Zenon and was later repaired by the Seljuk Turks, before being converted into a palace in the 13th century.
The document describes a study that evaluated a new combined method for detecting Listeria monocytogenes in environmental and food samples using ActeroTM Listeria Enrichment Media followed by detection with the DuPontTM BAX® System Real-Time PCR assay. The study compared the new method to USDA-FSIS MLG 8.09 and US FDA BAM 10 reference methods using inoculated samples of various foods and surfaces. The results demonstrated that the new combined method performed statistically equivalent or superior to the reference culture methods, with significantly reduced time to detection of L. monocytogenes. Independent laboratory validation studies further confirmed the high accuracy and reliability of the new method.
Empower Digital Skills for Good
Reach out to Asia Empower 2016
Innovation for Youth Social Entrepreneurship
Doha Qatar
March 17 - 19th
Workshop on March 18th co-hosted by QCRI and UNDP
Presentation by Heather Leson, Jennifer Colville, Ji Kim Lucas and Irina Temnikova
Event details:
https://www.reachouttoasia.org/event-details/empower-2016
El documento describe un proyecto para mejorar el aprendizaje de idiomas mediante el uso de smartphones. El proyecto consistió en desarrollar una aplicación llamada Terminkalender que permite a los estudiantes programar actividades en lengua extranjera con compañeros de manera anónima. Las pruebas piloto mostraron que la aplicación facilita la interacción entre estudiantes y permite al profesor monitorizar el proceso de aprendizaje.
This document provides an overview of NEMUS Bioscience, a biotech company focused on developing cannabinoid-based therapies. Some key points:
- NEMUS is developing therapies using cannabinoids for diseases like glaucoma, cancer, and antibiotic-resistant infections, leveraging 47 years of research from a partner university.
- Their pipeline includes a THC prodrug (NB1111) for glaucoma entering validation studies, and CBD derivatives for chemotherapy-induced nausea and neuropathy.
- Recent milestones include completing a $5M financing, adding experts to their scientific board, initiating programs for glaucoma and chemotherapy side effects, and signing a manufacturing agreement for lead programs.
This document is an investor presentation for NEMUS Bioscience, an OTCQB-listed biotech company developing cannabinoid-based therapies. Some key points:
- NEMUS has a proprietary pipeline led by NB1111, a THC prodrug for glaucoma, and novel CBD derivatives for retinal diseases and chemotherapy side effects.
- Recent milestones include completing a $5M financing, adding experts to their scientific advisory board, partnering with Athyrium to advance programs, and validating NB1111 data showing a 45% reduction in eye pressure.
- NEMUS' cannabinoid prodrug programs have a competitive advantage over orally administered cannabinoids, which
Nemus Bioscience is developing novel cannabinoid-based therapeutics for global medical challenges. It has an exclusive relationship with the University of Mississippi to develop cannabinoid compounds and targets. Its lead product NB1111 is a prodrug of THC being developed for glaucoma, a large global market with high unmet need. Preclinical studies show NB1111 significantly reduces eye pressure and may protect optic nerve cells, outperforming THC. Nemus aims to become a leading developer of second and third generation cannabinoid medicines.
The presentation summarizes IntelGenx, a drug delivery company focused on oral thin film technologies. It discusses IntelGenx's strategy to develop and commercialize improved drug delivery products using its oral thin film platform. Key points include successful commercial partnerships, a robust product pipeline including generic and branded products, positive clinical trial results, and a new manufacturing facility positioned for growth. Financial results show increasing revenue and adjusted EBITDA. The presentation positions IntelGenx as a leader in oral thin films with innovative technology and a clear strategy for growth.
The document is an investor presentation by IntelGenx, an innovative drug delivery solutions company. It summarizes the company's business strategy, product pipeline, and financial performance. Key points include IntelGenx's focus on repurposing drugs using its oral thin film technology, its partnerships with companies like RedHill and Chemo, its pipeline of products including treatments for migraines and erectile dysfunction, and the construction of its new manufacturing facility. The presentation highlights IntelGenx's potential for growth in the oral thin films market.
TGA presentation: Update on recent activitiesTGA Australia
This document provides an update on recent activities and ongoing reforms from the Scientific Evaluation Branch of the Therapeutic Goods Administration of Australia. It discusses implemented reforms such as streamlined variations for prescription medicines, utilizing evaluation reports from comparable overseas regulators, and biological and biosimilar medicines naming. Upcoming reforms addressed include improved labeling of neuromuscular blocking agents and regulation of fecal microbiota transplantation material. Approval times for different categories of medicines over the past years are also presented.
Discovery of Drug and Introduction to Clinical Trial_Katalyst HLSKatalyst HLS
Introduction to Discovery of Drug and Introduction to Clinical Trials in Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
IntelGenX Investor Presentation March 30 2017 ItelGenx
The presentation provides an overview of IntelGenx Corp, an innovative drug delivery company. It discusses IntelGenx's product pipeline including oral thin film versions of migraine, erectile dysfunction, and schizophrenia drugs. It also highlights a repurposed montelukast film for mild cognitive impairment currently in clinical trials. The presentation outlines IntelGenx's business strategy, partnership with Chemo, new manufacturing facility, and management team. It concludes that IntelGenx has a solid platform for growth due to its significant market potential and ability to build strategic partnerships.
This investor presentation provides an overview of IntelGenx Corp., an innovative drug delivery solutions company. It discusses IntelGenx's product pipeline including oral thin film versions of migraine, erectile dysfunction, and schizophrenia/bipolar drugs. The presentation highlights IntelGenx's strategic partnerships, new manufacturing facility, strengthened management team, and financial performance over recent years. It positions IntelGenx for continued growth by leveraging its drug delivery platform and oral thin film technology.
The document discusses the benefits of exercise for mental health. Regular physical activity can help reduce anxiety and depression and improve mood and cognitive functioning. Exercise causes chemical changes in the brain that may help boost feelings of calmness and well-being.
Daniel Sheline completed a co-op term at Toyota Technical Center from January to May 2007. During this term, he supported the ED2 470L vehicle design team and worked on several projects. He improved his CATIA and engineering design skills, learned Toyota's product development process, and strengthened his desire to have a career in automotive design.
The Next Million
ESA Earth Observation Summer School
Frascati (Rome), Italy
August 8, 2016
Summary: how can we get more people involved applying technical and research skills to tackle the SDGs. Includes extensive notes.
https://earth.esa.int/web/eo-summer-school/home1
Aspendos was an ancient Greek city founded around 1000 BC in Asia Minor that grew wealthy through trade. In the 5th century BC it became the most important city in the region of Pamphylia. It surrendered to the Roman Empire in 190 BC, after which the Romans pillaged its artistic treasures. The theater was built in 155 AD by the Greek architect Zenon and was later repaired by the Seljuk Turks, before being converted into a palace in the 13th century.
The document describes a study that evaluated a new combined method for detecting Listeria monocytogenes in environmental and food samples using ActeroTM Listeria Enrichment Media followed by detection with the DuPontTM BAX® System Real-Time PCR assay. The study compared the new method to USDA-FSIS MLG 8.09 and US FDA BAM 10 reference methods using inoculated samples of various foods and surfaces. The results demonstrated that the new combined method performed statistically equivalent or superior to the reference culture methods, with significantly reduced time to detection of L. monocytogenes. Independent laboratory validation studies further confirmed the high accuracy and reliability of the new method.
Empower Digital Skills for Good
Reach out to Asia Empower 2016
Innovation for Youth Social Entrepreneurship
Doha Qatar
March 17 - 19th
Workshop on March 18th co-hosted by QCRI and UNDP
Presentation by Heather Leson, Jennifer Colville, Ji Kim Lucas and Irina Temnikova
Event details:
https://www.reachouttoasia.org/event-details/empower-2016
El documento describe un proyecto para mejorar el aprendizaje de idiomas mediante el uso de smartphones. El proyecto consistió en desarrollar una aplicación llamada Terminkalender que permite a los estudiantes programar actividades en lengua extranjera con compañeros de manera anónima. Las pruebas piloto mostraron que la aplicación facilita la interacción entre estudiantes y permite al profesor monitorizar el proceso de aprendizaje.
This document provides an overview of NEMUS Bioscience, a biotech company focused on developing cannabinoid-based therapies. Some key points:
- NEMUS is developing therapies using cannabinoids for diseases like glaucoma, cancer, and antibiotic-resistant infections, leveraging 47 years of research from a partner university.
- Their pipeline includes a THC prodrug (NB1111) for glaucoma entering validation studies, and CBD derivatives for chemotherapy-induced nausea and neuropathy.
- Recent milestones include completing a $5M financing, adding experts to their scientific board, initiating programs for glaucoma and chemotherapy side effects, and signing a manufacturing agreement for lead programs.
This document is an investor presentation for NEMUS Bioscience, an OTCQB-listed biotech company developing cannabinoid-based therapies. Some key points:
- NEMUS has a proprietary pipeline led by NB1111, a THC prodrug for glaucoma, and novel CBD derivatives for retinal diseases and chemotherapy side effects.
- Recent milestones include completing a $5M financing, adding experts to their scientific advisory board, partnering with Athyrium to advance programs, and validating NB1111 data showing a 45% reduction in eye pressure.
- NEMUS' cannabinoid prodrug programs have a competitive advantage over orally administered cannabinoids, which
Nemus Bioscience is developing novel cannabinoid-based therapeutics for global medical challenges. It has an exclusive relationship with the University of Mississippi to develop cannabinoid compounds and targets. Its lead product NB1111 is a prodrug of THC being developed for glaucoma, a large global market with high unmet need. Preclinical studies show NB1111 significantly reduces eye pressure and may protect optic nerve cells, outperforming THC. Nemus aims to become a leading developer of second and third generation cannabinoid medicines.
The presentation summarizes IntelGenx, a drug delivery company focused on oral thin film technologies. It discusses IntelGenx's strategy to develop and commercialize improved drug delivery products using its oral thin film platform. Key points include successful commercial partnerships, a robust product pipeline including generic and branded products, positive clinical trial results, and a new manufacturing facility positioned for growth. Financial results show increasing revenue and adjusted EBITDA. The presentation positions IntelGenx as a leader in oral thin films with innovative technology and a clear strategy for growth.
The document is an investor presentation by IntelGenx, an innovative drug delivery solutions company. It summarizes the company's business strategy, product pipeline, and financial performance. Key points include IntelGenx's focus on repurposing drugs using its oral thin film technology, its partnerships with companies like RedHill and Chemo, its pipeline of products including treatments for migraines and erectile dysfunction, and the construction of its new manufacturing facility. The presentation highlights IntelGenx's potential for growth in the oral thin films market.
TGA presentation: Update on recent activitiesTGA Australia
This document provides an update on recent activities and ongoing reforms from the Scientific Evaluation Branch of the Therapeutic Goods Administration of Australia. It discusses implemented reforms such as streamlined variations for prescription medicines, utilizing evaluation reports from comparable overseas regulators, and biological and biosimilar medicines naming. Upcoming reforms addressed include improved labeling of neuromuscular blocking agents and regulation of fecal microbiota transplantation material. Approval times for different categories of medicines over the past years are also presented.
Discovery of Drug and Introduction to Clinical Trial_Katalyst HLSKatalyst HLS
Introduction to Discovery of Drug and Introduction to Clinical Trials in Pharmaceuticals, Bio-Pharmaceuticals, Medical Devices, Cosmeceuticals and Foods.
IntelGenX Investor Presentation March 30 2017 ItelGenx
The presentation provides an overview of IntelGenx Corp, an innovative drug delivery company. It discusses IntelGenx's product pipeline including oral thin film versions of migraine, erectile dysfunction, and schizophrenia drugs. It also highlights a repurposed montelukast film for mild cognitive impairment currently in clinical trials. The presentation outlines IntelGenx's business strategy, partnership with Chemo, new manufacturing facility, and management team. It concludes that IntelGenx has a solid platform for growth due to its significant market potential and ability to build strategic partnerships.
This investor presentation provides an overview of IntelGenx Corp., an innovative drug delivery solutions company. It discusses IntelGenx's product pipeline including oral thin film versions of migraine, erectile dysfunction, and schizophrenia/bipolar drugs. The presentation highlights IntelGenx's strategic partnerships, new manufacturing facility, strengthened management team, and financial performance over recent years. It positions IntelGenx for continued growth by leveraging its drug delivery platform and oral thin film technology.
Discovery of Drug and Introduction to Clinical Trial__Katalyst HLSKatalyst HLS
This document provides an overview of the drug discovery and clinical trials process. It discusses the goals of drug discovery which include identifying new chemical entities and developing medicines to address unmet medical needs. The drug discovery process involves target identification, validation, lead generation, and optimization. Pre-clinical testing is then conducted to evaluate safety and effects. If successful, an investigational new drug application is filed with the FDA prior to beginning clinical trials. Clinical trials involve 4 phases to test safety and efficacy in humans. Upon completion, a new drug application can be filed for FDA review and potential approval.
This investor presentation provides an overview of IntelGenx Corp., an innovative drug delivery solutions company. It discusses IntelGenx's pipeline of oral thin film products, including products for migraines, erectile dysfunction, schizophrenia/bipolar disorder, and mild cognitive impairment. The presentation highlights IntelGenx's strategic partnerships, new manufacturing facility, strengthened management team, and recent financial performance. It concludes that IntelGenx has established a solid platform for growth by leveraging its oral thin film technology and implementing a product sourcing strategy to identify high-value opportunities.
- IntelGenx Corp is a drug delivery company focused on oral film technologies. They have a pipeline of products using their VersaFilm and AdVersa drug delivery platforms.
- They have a state-of-the-art manufacturing facility in Montreal approved by Health Canada. Their pipeline includes products for migraine, erectile dysfunction, schizophrenia, and neurodegenerative diseases.
- They are conducting clinical trials for a Montelukast VersaFilm to treat cognitive impairment associated with neurodegenerative diseases like Alzheimer's, with promising preclinical and Phase I results shown.
Application for New Drug Discovery (NDD) according to USFDA guidelines Bharathiar university
The document discusses the US FDA's process for approving new drug applications (NDAs). The FDA is responsible for ensuring drugs are safe, effective and quality-controlled. Developers must submit clinical data to FDA's Center for Drug Evaluation and Research which reviews the data. If benefits outweigh risks, the drug receives approval. For serious conditions, accelerated approval is possible where post-market studies confirm initial findings. Designations like Fast Track can expedite review of innovative drugs that address unmet needs. A complete NDA includes manufacturing and clinical information. Advisory committees provide recommendations to FDA on approval.
Intelgenx Investor Presentation - July 6 2016ItelGenx
This document is an investor presentation for Innovative Drug Delivery Solutions that discusses the company's forward-looking statements and oral thin film drug delivery technology. It summarizes the market opportunities for oral thin films in treating conditions like migraines, erectile dysfunction, and opioid dependence. The presentation outlines IntelGenx's product pipeline including marketed products like Forfivo XL and products in development stages. It also discusses the company's new manufacturing facility, management team additions, and financial results that demonstrate its transformation into a growth-oriented company well positioned in oral thin film drug delivery.
Evaluating the cost to benefit ratio of a Drug Delivery platformBhaswat Chakraborty
This document discusses evaluating the cost to benefit ratio and end user benefits of drug delivery platforms. It covers understanding patient needs and formulation issues, benefits of matching needs and convenience, categories of drug delivery technologies, assessing cost to benefit ratios, and determining selection parameters. An example is given of an economic analysis showing a fentanyl transdermal system had the highest expected quality-adjusted life-days at a nominal increased cost compared to other long-acting oral opioids. The concluding remarks emphasize understanding needs, matching specific technologies to needs and formulations, relevance of therapeutic categories, and the importance of cost effectiveness and cost utility analyses.
The document discusses the complex and unpredictable nature of the FDA drug approval process. While the steps of drug development may seem formulaic, including discovery, preclinical testing, and clinical trials, success is not guaranteed as programs face many risks and intangible factors. Understanding these challenges is important for mitigating risks and strategizing development approaches. The FDA approval process aims to ensure new drugs are safe and effective for patients.
its not my personal work presentation but taken from lecture ppt from university of San Diego, california.
Its about the drug discovery process, its development and its commercialization.
This document is an investor presentation for Innovative Drug Delivery Solutions that discusses the company's forward-looking statements and drug delivery platforms. It summarizes the market opportunities for oral thin films, highlights the company's product pipeline including approved products and products in development, and describes their strategy to focus on developing products using oral films that provide benefits to patients. Financial results for 2015 and Q1 2016 are also presented, which demonstrate record results and an improving financial position as the company executes its strategy.
Ind (investigational new drug application) and ndaswati2084
The document provides an overview of the Investigational New Drug Application (IND) and New Drug Application (NDA) processes for bringing new drugs to market. It describes how an IND must be submitted to the FDA to test an experimental drug in humans, and outlines the types of INDs, content requirements, and review process. An NDA contains extensive clinical trial data and is required for FDA approval to commercially market a new drug. The lengthy and costly process from initial research to marketing approval averages 15 years and $900 million per new drug.
The document discusses the regulatory process for investigational new drugs (INDs) and new drug applications (NDAs) in the United States. It provides details on the types of INDs (investigator, emergency use, treatment), categories (commercial, research), required contents of an IND application, and FDA's Pre-IND consultation program. It also summarizes the purpose and required contents of an NDA to obtain approval to market a new drug in the US. Laws, regulations, guidance documents, and procedures that FDA follows in regulating drugs are also referenced.
Methanex is the world's largest producer and supplier of methanol. We create value through our leadership in the global production, marketing and delivery of methanol to customers. View our latest Investor Presentation for more details.
ZKsync airdrop of 3.6 billion ZK tokens is scheduled by ZKsync for next week.pdfSOFTTECHHUB
The world of blockchain and decentralized technologies is about to witness a groundbreaking event. ZKsync, the pioneering Ethereum Layer 2 network, has announced the highly anticipated airdrop of its native token, ZK. This move marks a significant milestone in the protocol's journey, empowering the community to take the reins and shape the future of this revolutionary ecosystem.
Cleades Robinson, a respected leader in Philadelphia's police force, is known for his diplomatic and tactful approach, fostering a strong community rapport.
UnityNet World Environment Day Abraham Project 2024 Press ReleaseLHelferty
June 12, 2024 UnityNet International (#UNI) World Environment Day Abraham Project 2024 Press Release from Markham / Mississauga, Ontario in the, Greater Tkaronto Bioregion, Canada in the North American Great Lakes Watersheds of North America (Turtle Island).
2. 2
Forward Looking Statement
This presentation contains “forward-looking statements” within the meaning of the “safe harbor” provisions of
the Private Securities Litigation Reform Act of 1995. All of the statements in this presentation, whether written or
oral, that refer to expected or anticipated future actions and results of NEMUS Bioscience, Inc. (NEMUS) are
forward-looking statements. These forward-looking statements reflect the beliefs and expectations of the
management of NEMUS as of the date of this presentation. NEMUS cannot give any assurance that such forward-
looking statements will prove to be correct. The reader is cautioned not to place undue reliance on these forward-
looking statements.
The information provided in this presentation does not identify or include any risk or exposures, of NEMUS that
would materially adversely affect the performance or risk of the company. For a description of the risks and
uncertainties related to the business of NEMUS, see our Annual Report on Form 10-K for the year ended
December 31, 2014 filed with the Securities and Exchange Commission on March 27, 2015 and our subsequent
periodic reports filed with the Securities and Exchange Commission.
All information contained in this presentation is provided as of the date of the presentation and is subject to
change without notice. Neither NEMUS, nor any other person undertakes any obligation to update or revise
publicly any of the forward-looking statements set out herein, whether as a result of new information, future
events or otherwise, except as required by law. This presentation does not convey an offer of any type and is not
intended to be, and should not be construed as, an offer to sell, or the solicitation of an offer to buy, any securities
of NEMUS.
3. 3
OTCQB NMUS
Price (10/2/15) $0.70 (15 day historical ave.)
Market Cap (10/2/15) $12.65 M
Shares Outstanding
18.1 M common & 5000 PS,
24.3M if 100% converted
% Ownership by Directors &
Employees
23.2% shares
1.13 M options
Warrants Outstanding 10.6 M (Avg. Strike @ $1.15)
Founded 2012
Base of Operations
Costa Mesa, California
& Oxford, Mississippi
Company Overview
NEMUS Bioscience is a publicly traded, life-science biotech company,
developing regulatory-approved, cannabinoid-based therapies, for a
spectrum of diseases, especially those of unmet medical need
4. 4
NEMUS Investment Highlights
• Proprietary product pipeline led by a new chemical entity, a pro-drug of
tetrahydrocannbinol or THC (NEMUS product candidate: NB1111)
• Patent issued for composition of matter, production, and methods of use
using a variety of formulations/combinations
• The lead compound, NB1111 is a first-in-class treatment for glaucoma
• NEMUS is the only partner of the University of Mississippi for discovery,
research and commercialization of cannabinoid-based medicines
• The University of Mississippi is the only U.S. entity authorized by the Federal
government since 1968 to cultivate cannabis for research for the study of over
100 cannabinoid molecules in the plant
• NEMUS management team has proven track-record in drug research,
pharmaceutical & biotech development, and public company experience on a
global scale
5. 5
Recent Milestones
• August, 2015: Completion of Series B $5 million financing round
• September, 2015: Robert N. Weinreb, globally recognized glaucoma expert joins
NEMUS Scientific Advisory Board; Chairs Ophthalmology Board
• September, 2015: Testing completed of ocular delivery vehicle for targeted
once-daily dosing of lead NEMUS compound for glaucoma (NB1111; prodrug of
THC)
• October, 2015: Testing continues of cannabidiol (CBD) prodrugs designed for
ophthalmic and systemic use
• October, 2015: NEMUS partners with Atheln to advance multiple development
programs; Dr. Judy Gordon, pre-eminent ophthalmology regulatory expert to
oversee NEMUS ophthalmology FDA relationship
• October, 2015: rabbit glaucoma study initiated assessing vehicle delivery of
NB1111 in an animal disease model to assess half-life, efficacy, and safety
6. 6
Currently approved cannabinoids have poor
bioavailability & poorly predictable pharmacokinetics
Oral cannabinoids (both pill and spray delivery mechanisms) are subject to high
Patient-to-patient variability
• Metabolism can vary based on an individual’s genetic metabolic profile
• Plasma levels can be influenced by other medications
• Drug levels impacted by what a patient has eaten
– “Due to extensive first-pass metabolism and high lipid
solubility, a fraction of the drug reaches the circulation”1
– “The pharmacologic effects of Marinol are dose-related
and subject to considerable inter-patient variability”1
– “Intoxication type reactions appear dose-related due to
great inter-patient drug level variability”2
– “The pharmacokinetic data show great inter-subject
variability”3
1) Marinol Summary Basis of Approval
2) Sativex Product Labelling - Black Box Warning
3) Sativex Product Labelling
NEMUS will capitalize on the
use of proprietary formulations
that could allow for alternative
delivery methods
7. 7
Goal: Predictable Cannabinoid
Bioavailability & Pharmacokinetics
NEMUS has licensed a new chemical entity and formulations that
have shown improved delivery of cannabinoids in pre-clinical testing
Ocular Trans-mucosal Rectal
-1
4
9
PD 1 3 5 7 9 11 13 15 17 19 21 23
PlasmaConcentrations
(ng/ml)
Timepoint (h)
A Comparison of THC Plasma Concentrations From
ProDrug THC Suppository* vs. Marinol in Humans
Marinol 10 mg THC 10 mgEg
Source: NEMUS Internal Data -
All NEMUS licensed
delivery options avoid
bioavailability-
compromising first-pass
metabolism by the liver
8. 8
• The Single Convention treaty requires member nations (over 100) to designate a single
entity eligible to cultivate cannabis for research purposes
• The University of Mississippi is the only entity in the US that is authorized by NIDA
and the DEA to cultivate cannabis on behalf of the federal government
• The University of Mississippi has a continuous 35+ year regulatory history in dealing
with FDA, DEA, NIDA, NIH, etc.
• A January 22, 2013, U.S. Court of Appeals for the District of Columbia Circuit upheld
DEA’s continued classification of cannabis as a Schedule I controlled substance,
subject to stringent regulation
• In March, 2015, NIDA once again granted the 5yr contract to the University
• This also presents hurdles to the development, commercialization and importation of
products into the U.S.
The Only Federally-Approved Source of
Cannabis-Derived Compounds
9. 9
NEMUS and the University of Mississippi: Over 45 years
of Intellectual Capital in Cannabinoid Chemistry
Recurring Option Agreement for the NCE
UM 5050 – THC Ester – Recurring option agreement on any use of THC ester. (Patent issued in Aug, 2014)
Method of Delivery Agreements
UM 4718 – Suppository Delivery of Dronabinol Hemisuccinate (DHS) – Exclusive worldwide license to intellectual
property, proprietary data and know-how related to a suppository dosage form containing Dronabinol
Hemisuccinate and other esters. (“NPC 4718”) and development through FDA.
UM 1490 – TransMucosal Delivery of Cannabinoids – Exclusive worldwide license to intellectual property,
proprietary data and know-how related to transmucosal delivery of cannabinoids (“UM1490”) and development
through FDA.
UM 8790 – Ocular Delivery of Cannabinoids – Exclusive worldwide license to intellectual property, proprietary data
and know-how related to ocular delivery of cannabinoids (“UM 8790”) and development through FDA.
Research Agreement
UM 5070 – MRSA – Exclusive worldwide option to license intellectual property, proprietary data and know-how
related to the treatment of methicillin-resistant Staphylococcus aureus infections using cannabinoids (“UM
5070”) and development through FDA.
CBD Pro-drug – Exclusive worldwide option to license intellectual property, proprietary data and know-how on the
use of a proprietary cannabidiol prodrug.
EXCLUSIVE AGREEMENTS BETWEEN NEMUS AND THE UNIVERSITY OF MISSISSIPPI
10. 10
Key Partnership With University Of Mississippi and
International Thought Leaders in Ophthalmology
• NEMUS has licensed the rights to a novel THC pro-drug. The recently issued patent contains claims for
composition of matter, formulation, delivery and method of use
• NEMUS has entered into multiple license agreements and a research agreement for specific
formulations and corresponding delivery methods
• NEMUS has perpetual, worldwide exclusivity for all compounds and targets we are working on with UM
• UM provides over 45 years of knowledge and experience in the science of cannabinoids
• NEMUS has access to a large number of globally recognized scientists and thought leaders in
cannabinoid medicine
• Robert Weinreb, MD; Distinguished Professor of Ophthalmology; renown expert in glaucoma
• Dr. Judy Gordon; pre-eminent regulatory specialist in ophthalmology
11. 11
NEMUS Licensed the Rights from UOM
US Patent : 8,809,261
• Issued Aug 19, 2014 to University of Mississippi.
• Compositions containing delta-9-THC-amino acid
esters and process of preparation.
• Consists of 66 claims:
– Amino acid, hemi-succinate, hemi-gluturate forms
of THC.
– Preparation of several forms of amino acid, hemi-
succinate, and hemi-gluturate forms of THC.
– Compositions that contain forms of amino acid,
hemisuccinate, and hemi-gluturate forms of THC.
– “Any condition that can respond to the prodrugs
of delta-9-THC in a pharmaceutically acceptable
carrier.”
12. 12
Development Pipeline: Near-, Intermediate-, Longer-
Term Projects; CBD formulations in development
Drug Name Target Research Pre-clinical Phase 1 Phase 2 Phase 3
NB1111
Glaucoma/Ophthalm
ology Targets
Topical
Ocular
Delivery
NB2221
Multiple Sclerosis
Spasticity
NB51R1 Anxiety
Buccal
Patch or
Suppository
Delivery
NB23R1 Epilepsy
NB31R1
Methicillin-Resistant
Staph Aureus
Cannabinoid Cocktail
Anti-
Infective
In parallel to the THC program which is entering preclinical IND-enabling studies, NEMUS is also preparing
development tracts for other biologically active cannabinoids, including but not limited to CBD
Target indications are multi-billion dollar global markets of urgent medical need
14. 14
Our Strategic Asset Management evaluation concluded
that glaucoma was the most attractive first target
• $8 billion globally and growing with aging populations
• A leading cause of blindness in the US
• $2.3 billion US market (32 MM Rx)
• Regulatory pathway well-defined
• Regulatory strategy: Potential for “urgent medical need”
and “breakthrough therapy” FDA designations;
• Glaucoma as a “Non-responder” market presents greater
opportunities; >50% of patients on 2 or more Rx
• Cannabinoids have shown neuroprotective qualities in
vitro and in vivo (multiple animal species)
• Licensing and acquisitions in the glaucoma market occur
predominantly earlier in development (pre-clin, phase 1)
15. 15
Lead Compound: NB1111 (Glaucoma/Ophthalmology)
Topical ocular treatment with a proprietary THC prodrug could bring a new
therapeutic class directly to the target organ, avoiding systemic exposure
FEATURES OF THE NEMUS LEAD COMPOUND
• Penetrates all chambers of the eye
• Produces a reduction in Intra-Ocular Pressure (IOP) in
glaucoma animal model (THC has been shown to lower
IOP in previous human testing)
• Reduction of IOP is the only proven method to treat
glaucoma
• QD dosing objective using new delivery mechanism
• Potentially first medication to exert direct
neuroprotection of the optic nerve (retinal ganglion
cells; RGCs) by inhibiting apoptosis pathway
• Neuroprotection is the “holy grail” of glaucoma
The proprietary formulation
allows THC to be absorbed
across membranes that are
normally barriers to
absorption.
16. 16
Only NB1111 addresses multiple MOAs
Therapy Class
Mechanism of
Action (MOA)
Increased flow
Trabecular mesh
Increased flow
uveoscleral
pathway
Decreased fluid
production
Direct
neuroprotective
qualities
Prostaglandins
(50% mkt share)
X
β- adrenergic
blockers (30%)
X
α- adrenergic
agonists (10%)
X X
Carbonic
anhydrase
inhibitors (<5%)
X
Cholinergic
agonists (<5%)
X
Pro-drug THC
(NB1111)
X X X X
17. 17
THC lowers IOP in humans; predictive animal model
consistent with human experience
• Active moiety of NB1111, THC, has been shown to lower IOP in
humans
• Testing conducted by universities, NIH, and the US Army
• THC component of proprietary pro-drug lowered IOP in human
glaucoma up to 65% in some cases
• The NEMUS prodrug NB1111 achieved a 45%-50% reduction in IOP
in a validated rabbit glaucoma model
• Rabbit glaucoma model presented at AAPS meeting November,
2014 by University of Mississippi
• New formulation testing of NB1111 to enhance half-life: QD dosing
18. 18
THC-val-HS outperforms timolol and
pilocarpine in IOP reduction*
18
* Bhagav P, et al. Development of Δ9-tetrahydrocannabinol prodrug
and improved IOP lowering efficacy; AAPS Poster Session, November,
2014
19. 19
Unlike many licensing deals, ophthamology deals are
often done early in development
0
10
20
30
40
50
60
70
80
Ophthalmology deals Related to Pharmaceuticals
n=265 2007-2014
Acq/purchase
License
Of 408 deals related to ophthalmology revealed in SEC documents, 265 were
related to pharmaceuticals, from early to late stage.
20. 20
Value grows after Phase 1 and again after Phase 2
(ex, glaucoma @ $750MM peak year)
21. 21
Q2 2015 Q3 2015 Q4 2015 Q1 2016 Q2 2016 Q3 2016 Q4 2016 Q1 2017 Q2 2017 Q3 2017
NB1111 Development Timeline: Glaucoma
CMC & Formulation
Clinical Batch Production
IND Enabling Studies
File IND
FPI
Clinical Site
Contracting
Phase 1b/2a Study
LPO
22. 22
Use of proceeds: glaucoma
ACTIVITY PROJECTED COST
CMC*-FORMULATION $2.6 million
IND** ENABLING STUDIES & FILING $3.2 million
CLINICAL PHASE 1b/2a Study $1.8 million
PROJECTED TOTAL $7.6 million
24. 24
Methicillan-Resistant Staph Aureus (MRSA)
MRSA FACTS & CURRENT MEDICAL LANDSCAPE
• First described in 1961 now a pandemic
• CDC: prevalence of MRSA in ICU setting approaching 60%
• 1960’s: one genetic MRSA mutation/clone; currently six
MRSA genetic clones; 15 clones in China
• 2010 hospital survey: 61.8% of patients admitted to ICU were
MRSA colonized1
• 50% of screened patients had healthcare-associated
infections1
• 11,000 deaths annually; 80,000 invasive infections/yr.2
• Annual costs in the US: $3.2 - $4 billion2
1) Jarvis WR et al; Am J Infect Control 2012; 40(3): 194-200
2) Pew Trust MRSA Survey; April 3, 2012
25. 25
Methicillan-Resistant Staph Aureus (MRSA)
NEMUS is assessing a new class of anti-infectives to combat the threat of
antibiotic resistance
CANNABINOID EXPERIENCE IN MRSA1
• Select cannabinoids have been known to possess some antibacterial properties 1
• Anti-bacterial properties can be leveraged to address newly developed strains exhibiting antibiotic
resistance to current meds
• NEMUS intends to file IP concerning the use of transmembrane enhancing formulations of
cannabinoids to facilitate bacteriocidal activity
• IP is being developed on the use of “drug cocktails” to address certain species of MRSA and other
bacterial species so that therapy can be tailored to specific strains, in an effort to lower resistance
development going forward
1) J Nat Prod. 2008 Aug;71(8):1427-30. doi: 10.1021/np8002673. Epub 2008 Aug 6.
- Antibacterial cannabinoids from Cannabis sativa: a structure-activity study
26. 26
Product Development Strategy
NEMUS will initially operate through a strategically aligned network of researchers, CMC consulting
experts, and specialty service consultants to advance our pipeline projects
• Strategic direction
• Clinical/regulatory responsibility
• Legal/IP
• Management of partners
• Business development
• Commercialization in selected
markets
• IP and Discovery
University of
Mississippi
•UCSD
•Johns Hopkins
•University of Washington
Academic
Research Partners
•Develop and execute IP strategyLegal/IP Partner
•Drug development/tech transfer
Atheln and/or
other out-sourced
CMO/CRO firm
•ManufacturingAPI
•Commercialization Partners
•Out-licensing Assessment
Pharma/Biotech
27. 27
Management
COSMAS N. LYKOS, ESQ – Co-founder, Officer & Board Member – Executive Chairman
Cosmas Lykos co-founded NEMUS in 2012 and has served as its Chairman of the Board of Directors since August
2014. After graduating with Honors from Duke University School of Law in 1993, Mr. Lykos began his career at Gibson
Dunn & Crutcher, LLP, an international full-service law firm, as a corporate associate until 1998. From 1998 to 2004, Mr.
Lykos served as Vice President of Business Affairs, General Counsel, Secretary and Chief Compliance Officer
of RemedyTemp, Inc., a NASDAQ publicly-traded temporary staffing firm with over 250 directly-owned and franchised
offices nationwide. From 2004 until 2008, Mr. Lykos served as Vice President of Business Development, Chief Legal Officer,
Secretary and Chief Compliance Officer of Oakley, Inc., a NYSE publicly-traded sports and technical eyewear, apparel,
accessories and retail company. In January of 2008, he became Co-owner and President of the Optical Shop International,
a designer and distributor of licensed eyewear brands, including Chrome Hearts and Blinde, through two wholly-owned
foreign subsidiaries with a direct and distributor sales network in over 60 countries around the world. Primary
responsibilities included developing and implementing OSI’s vision and strategies and the management of its foreign
subsidiaries, sales, legal, human resources, finance and administrative functions. In 2011, Mr. Lykos negotiated and
consummated the sale of OSI to its primary licensor, Chrome Hearts LLC and continues to provide consulting services. Mr.
Lykos has extensive public and private company board of directors experience. As Chief Compliance and Legal Officer and
Secretary of both Oakley, Inc. and RemedyTemp, Inc., Mr. Lykos attended all board of director meetings and board
committee meetings. As an angel investor, Mr. Lykos has made minority investments in various private companies and has
served on their Board of Directors.
28. 28
Management
BRIAN MURPHY, MD, MPH, MBA – Chief Executive Officer; Chief Medical Officer, Director
Dr. Murphy has almost two decades of experience in drug development and evaluation, both from the academic and industry
perspective. He most recently served as the CMO of Eiger Biosciences. Previously, Dr. Murphy was CMO at Valeant
Pharmaceuticals International (VRX) where his responsibilities also included oversight of Global Medical Affairs and
Pharmacovigilance. Dr. Murphy also served as Medical Director, then VP of Marketing and Commercial Strategy of Hepatology
for InterMune, Inc. (ITMN). Prior to InterMune, Dr. Murphy was Medical Director of North America for Antivirals/Interferons at
Hoffmann-LaRoche. Murphy is board-certified in internal medicine and completed his residency at Tufts-New England Medical
Center. He went on to complete parallel fellowship tracts at Harvard Medical School and the Massachusetts General Hospital.
Dr. Murphy earned his MD, MPH (general public health), and MS (pharmacology) degrees from New York Medical College and is
a graduate of the Harvard School of Public Health (MPH in Health Policy and Management). He earned his MBA at the Columbia
University Graduate School of Business.
LIZ BERECZ, MA, CPA - Chief Financial Officer
Elizabeth Berecz is a seasoned financial executive with over 20 years of experience holding senior level positions in both private
and public companies. She has proven success in leading strategic planning, financial reporting, and global system
implementations for companies of various sizes. Liz started her career at Price Waterhouse Silicon Valley where she spent five
years auditing several high profile public companies in the technology industry. She then spent 10 years holding key leadership
positions in various publically held Companies including Quantum Corporation (Corporate Controller), Business Objects (VP
Finance and Administration), and Excite (VP Finance), followed by 10 years of key leadership roles in privately held Companies
including CFO positions with Optical Shop International, StarTrac Inc., Power Balance Technologies, Inc. and most recently
Bentley Mills, Inc. She also serves as an Adjunct Professor of Accounting and Finance at the University of San Francisco.
Elizabeth received her BA in Economics from Stanford University and a MA in Sports Management from University of San
Francisco.
29. 29
BOD & Strategic Advisors
MAHMOUD A. ELSOHLY, PHD
Scientific Advisor
World’s foremost expert on the science
of cannabinoids. 300+ scientific
publications . Research professor at The
University of Mississippi.
JERRY MCLAUGHLIN, MBA
Strategic Advisor,
Board of Directors - Member
25 year veteran executive in
pharmaceutical medical device and
healthcare related industries (AgeneBio,
Merck, Endo Pharma, Villanova
University, Dickinson College).
TOM GEORGE
Board of Directors – Chairman of Audit
Committee
30 year senior executive in corporate
finance and accounting (Deckers Brands,
Ophthonix, Oakley).
DOUGLAS S. INGRAM, ESQ
Board of Directors – Vice Chairman,
Chairman of Compensation Committee
25 year senior executive in healthcare,
Past President of Allergan, former
Attorney at Gibson, Dunn & Crutcher,
LLP. Summa cum laude and Order of the
Coif graduate of the Univ. of Arizona
school of law. Robert N. Weinreb, M.D.
Scientific Advisor
Chair, Ophthalmology Advisory Board
Globally recognized expert on glaucoma
and eye diseases. 1000+ scientific
publications. Distinguished Professor of
Ophthalmology; University of California
San Diego
Judy Gordon, D.V.M..
Scientific Advisor
Ophthalmology Regulatory Specialist
Pre-eminent regulatory specialist with
internationally recognized expertise in
regulatory filings at FDA/EMA for NCE’s
for use in the ophthalmology space
30. 30
Contact
650 Town Center Drive, Suite 1770
Costa Mesa, CA 92626
(949) 396-0330
hello@nemusbio.com
www.nemusbioscience.com
Investor Relations
Mike Cole, Vice President
MZ North America
Tel: 949-259-4988
mike.cole@mzgroup.us
www.mzgroup.us
Company
Brian Murphy, MD, MPH, MBA
CEO - CMO
Tel: 949-355-1140
brian@nemusbio.com