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Dr. Kamala Kalyani Maddali DVM, PhD



NAME:    Kamala Kalyani Maddali DVM , Ph.D.
Immigration status: Greencard holder
Address: 123 Springfield drive, Sellersville, PA, 18960
Phone: 215-257-2543 (Home)/980-339-2631 (Cell)


Email: KAMALAKMADDALI@GMAIL.COM



EDUCATION:


2010: CCRA, Medical Research Management Institute, Florida, USA.

2002-2005: Doctorate of Philosophy Ph.D. (Cardiovascular Pharmacology/Physiology), Biomedical
Sciences, University of Missouri, Columbia, MO

1995-2001: Doctorate in Veterinary Medicine DVM, Andhra Pradesh Agricultural University, India



PROFESSIONAL EXPERIENCE:

2008-2010: Translational Scientist, Huntingdon Life Sciences, Princeton Research Center, East
Millstone, NJ 08875

2005-2008: Research Associate- Pre clinical Development, Merck Research Laboratories, West Point,
PA 19486

2002-2005: Graduate Research Assistant, Dept of Biomedical Sciences, University of Missouri-Columbia,
MO 65211

2001: Intern Veterinarian, Veterinary Poly Clinic, Kurnool, AP, India-518001

DETAILED RESPONSIBILITIES:

Fields of experience:

Oncology/Cardiovascular/Diabetes/Neurology/Endocrine/Immunology


2008-2010: Translational Scientist, Huntingdon Life Sciences: This customer focused position acted
as a “Scientific Liaison” for biomarker selection and analysis by providing strong scientific link between
clients and analytical departments at Huntingdon Life Sciences’ UK and US facilities. Preclinical and
clinical biomarker analyses were undertaken by genomics, MRI-PET tracers, Veridex (circulating tumour
cells) CTCs, immunoassay, LC-MS, histopathology, mass spectrometry, and cell based assays.

Job Responsibilities:

        Biomarker advisory services:

    •   Play a pivotal role as a Preclinical and Clinical R&D advisor (GLP/GCP) in recommending
        biomarker/personalized medicine (diagnostics) strategies and applications based on sponsor's
        small molecule/biologics drug development programs.
    •   Translating scientific or clinical data into high quality medical information to help clinical
        investigators best design their drug development programs.



                                                                                                     1
Dr. Kamala Kalyani Maddali DVM, PhD



   •   Responsible for the creation and ownership of a biomarker work plan (for clinical protocols) for
       clinical and preclinical phases by interacting with healthcare professionals/pharmaceutical
       investigators/physicians etc.

   •   Project management with Pharma/biotech clients to best understand client project objectives and
       goals

   •   Implement pricing/new technology strategies globally with in the company

   •   Scientifically translate client needs into effective research plan

   •   Execute research plan as part of a team including survey design, data analysis, and structuring of
       presentations and also responsible for professional review of the published literature as well as
       other sources of information to provide team members with timely summaries and critical
       evaluations of advances in basic and clinical programs.

   Business Development activities: Act as a “consultant” in the following activities:

   •   Establish and maintains effective communication/coordination with sponsors, field sales, and
       managed market account representatives. Traveling to client sites and interacting with sponsors
       on a regular basis through     communications, publication planning, slide decks, manuscript
       publications and marketing case studies

   •   Works closely with the global director of marketing/sales in regard to biomarkers/personalized
       medicine on the management of diverse R and D programs.

   •    Stays abreast with literature in the field and contributes to case studies, pricing strategies,
       forecasting markets, proposal writing, and other strategic development efforts.

   •   Identifies, interacts and maintains relationships with consultants, vendors and KOLs in the arena
       of biomarkers/personalized medicine field involving pharmaceutical/biopharmaceutical clients.

   •   Represented HLS at several national scientific meetings (ASCO, DIA, SOT etc.). Business
       development through customized presentations and creating distinctive marketing materials for
       HLS Biomarker services.
   •   Matrix involvement with four “Analytical groups” with 6 PhD’s involving Flow
       cytometry/Immunoassay/Clinical Pathology/Mass Spec/Histopathology/Immunohistochemistry.

Process Improvements:
   •   Create a Business Biomarker Proposal Process for initial communication with the clients and a
       hand-off of the project to Operations group.
   •   Create a formal feedback mechanism for client communication and measurement of client
       satisfaction by initiating monthly "Process Improvement" meetings between Operations and
       Business Development.

2005-2008: Research Associate, Merck Research Laboratories



   1. Development of in vivo pharmacology and toxicity models that can be used to screen drug
       development candidates; leading to go/no-go decisions. Work with researchers on study designs
       during lead optimization of the drug development process. Experience working in the area of
       cancer (knock-out mice models), metabolic disorders (diabetes, obesity, atherosclerosis),
       cardiovascular, inflammatory diseases.




                                                                                                    2
Dr. Kamala Kalyani Maddali DVM, PhD



   2. Formulate and execute novel strategies to decrease attrition of drug development candidates due
        to toxicity.

   3. Plan experimental approaches (GLP/Non-GLP) to gain mechanistic understanding around safety
        signals observed in preclinical toxicity studies and place in context of human risk.

   4. Develop translatable biomarkers to effectively monitor and manage safety in humans.

   5. Identify the key routes to translate in vitro observations into whole animal studies to provide in
        vivo Proof of Concept/ Proof of Mechanism for novel therapeutic candidates.

   6. Identify efficacy markers (“biomarkers”) in animal models (oncology/endocrine/cardiovascular)
        which may be translatable into human studies and ensure that these are appropriately examined
        in translational approaches.

   7. Dotted line supervision of a laboratory (with 4-5 scientific staff) for biomarkers (Molecular Diag-
        nostics Lab) and training technical staff in newly introduced techniques (through IHC/RT-PCR/Lu-
        minex/Meso-scale/Veridex (CTCs); etc). Interactions with local lab leads & scientists from Discov-
        ery and Safety Assessment groups.

   8. Key role in the oncology, inflammatory and myotox biomarker committees tasked with the identifi-
        cation and validation of safety biomarkers.

   9. Translational animal model experience working in the area of oncology, neuroscience, metabolic
      disorders (diabetes, obesity, atherosclerosis), cardiovascular, endocrine disorders, inflammation,
      hypertension.

   a.   Oncology models
   b.   Neuroscience models-Alzhimers/Parkinsons/Sleep Apnea
   c.   Cardiovascular models- Atherosclerosis/Restenosis models
   d.   Obesity models – Primates- Rhesus, Cynologous Monkeys; Rats, Mice, Marmosets
   e.   Respiratory models-Cough model
   f.   Inflammatory models.


   10. Development, validation, and implementation of technologies that include:

        a.   Veridex/CTC
        b.   MRI/PET
        c.   FLIPR
        d.   MSD/Luminex
        e.   Flow Cytometry
        f.   LC-MS
        g.   Confocal microscopy
        h.   Electron microscopy
        i.   RT-PCR
        j.   Immunoprecipitation
        k.   Immunohistochemistry
        l.   Laser Capture Micro dissection
        m.   Western Blots



2002-2005: Graduate Research Assistant, University of Missouri-Columbia, MO 65211
Thesis Title: A Mandatory requirement of PKC-delta in testosterone regulated smooth muscle cell
differentiation, proliferation, and apoptosis

   •    Training in porcine and rat models of atherosclerosis and restenosis




                                                                                                     3
Dr. Kamala Kalyani Maddali DVM, PhD



    •   Investigated the role of inflammation and protein trafficking in coronary heart disease utilizing in
        vivo and ex-vivo porcine models and cell based assays
    •   Delineating the role of various cell cycle proteins (positive and negative cell cycle regulators), ap-
        optotic proteins, signalling pathways like PKC, MAP kinase, and lipid and lipoprotein metabolism
        in the regression of coronary plaques in porcine disease models.

    •   4 year extensive training in various in vivo and in vitro techniques such as primary cell cultures,
        western blots, flow cytometry, confocal microscopy, siRNA based gene knockouts, immunohisto-
        chemistry etc.

2001: Intern Research Veterinarian, Veterinary Poly Clinic, Kurnool, AP, India-518001

GRANTS AND AWARDS: 2005: American Heart Association Heartland Affiliate: $ 50,000
Grant Title: “Testosterone Regulation of Coronary Smooth Muscle Cell Differentiation and Proliferation”

PUBLICATIONS AND PRESENTATIONS:

     K.K. Maddali- “Invited speaker for Association of Inhalation Toxicology, Germany-Biomarkers in
        COPD”, October 2010.
     K.K. Maddali- “Invited speaker for AECCP, Verona, Italy-Translational strategies for cardiac
        biomarkers”, Sep 2010.
     K.K.Maddali, Sample processing and Biomarker analysis”. Webinar for ACRP, 2009.
     K.K. Maddali- “It is time to implement an early renal toxicity biomarker strategy”, Developments
        in Life Sciences (HLS internal journal), Vol. 9, No. 1.
     K. K. Maddali, C. I. Starks, C. McDonough, J. Dharmadhikari, B. A. Litzenberger Bone
      biomarkers significantly enhances the predictability of preclinical study outcomes and translation
      to first in man studies targeted towards osteoporosis. AACC National Meeting, 2009.
     KK Maddali, IT Rogers, SL Motzel D Connor H Klein Development of Cough model in Guinea
      Pigs National AALAS, Charlotte, NC 2007.
     KK Maddali, IT Rogers, SL Motzel D Connor, H Klein Development and validation of Biomarkers
      in Rhesus monkey model of Diet induced obesity, ENDO, Canada, 2007.
     D. K. Bowles, K. K. Maddali, V. C. Dhulipala, and D. H. Korzick PKC-delta mediates anti-
      proliferative, pro-apoptic effects of testosterone on coronary smooth muscle. Am J Physiol Cell
      Physiol, August 2007; 293(2): C805 - C813.
     KK Maddali, IT Rogers, SL Motzel D Connor, H Klein Metabalonomic markers in obesity
        monkey models, ENDO, San Diego, 2006.
     KK Maddali, DH Korzick, JR Turk and DK Bowles. Isoform-specific modulation of coronary PKC
        by glucocorticoids. Vascular Pharmacology. 2005 42:153-162.
     KK Maddali, DH Korzick, Tharp DL and DK Bowles. PKC-delta mediates testosterone-induced
        increases in coronary smooth muscle Cav1.2. J Biol Chem. 2005 Dec 30;280(52):43024-9. Epub
        2005 Oct 21.
       KK Maddali, Donna Korzick and Douglas K. Bowles. Testosterone alters coronary proliferation
        through PKC-delta mediated mechanism. Experimental Biology, 2005. FASEB J.
       KK Maddali, Donna Korzick and Douglas K. Bowles. Testosterone alters coronary apoptosis
        through PKC-i , delta mediated mechanism. Experimental Biology, 2005. FASEB J.
       Vamsidhara C. Dhulipala, KK Maddali, Wade V. Welshons and Chada S. Reddy. Effects of
        Secalonic acid-D toxin, on murine palatal mesenchymal cell cycle. Developmental and
        Reproductive Toxicology, Birth defects Journal, 2005, June ;74(3):233-42.
       Bowles DK, Cl Heaps, JR Turk, KK Maddali, EM Price. Hypercholesterolemia inhibits L-type
        calcium channel current in coronary macro-, not micro circulation. Journal of Applied
        Physiology, 2004 June; 96(6):2240-8.
       Bowles DK, KK Maddali, VK Ganjam, LJ Rubin, DL Tharp and CL Heaps. Endogenous
        testosterone increases L-type Ca2+ channel expression in porcine coronary smooth muscle.
        American Journal of Physiology – Heart and Circulatory Physiology, 2004 Nov;
        287(5):H2091-8.




                                                                                                         4
Dr. Kamala Kalyani Maddali DVM, PhD



    KK Maddali, Donna Korzick and Douglas K. Bowles. Testosterone alters coronary PKC- delta
     expression and PKC-mediated Voltage gated calcium channel expression, 6587, Experimental
     Biology, 2004.
    KK Maddali, Donna Korzick and Douglas K. Bowles. Effect of glucocorticoids on PKC isoform
     expression in porcine coronary arteries, 6330, Experimental Biology, 2003.

REFERENCES: Provided upon request




                                                                                         5

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Kamala Maddali Cv2011

  • 1. Dr. Kamala Kalyani Maddali DVM, PhD NAME: Kamala Kalyani Maddali DVM , Ph.D. Immigration status: Greencard holder Address: 123 Springfield drive, Sellersville, PA, 18960 Phone: 215-257-2543 (Home)/980-339-2631 (Cell) Email: KAMALAKMADDALI@GMAIL.COM EDUCATION: 2010: CCRA, Medical Research Management Institute, Florida, USA. 2002-2005: Doctorate of Philosophy Ph.D. (Cardiovascular Pharmacology/Physiology), Biomedical Sciences, University of Missouri, Columbia, MO 1995-2001: Doctorate in Veterinary Medicine DVM, Andhra Pradesh Agricultural University, India PROFESSIONAL EXPERIENCE: 2008-2010: Translational Scientist, Huntingdon Life Sciences, Princeton Research Center, East Millstone, NJ 08875 2005-2008: Research Associate- Pre clinical Development, Merck Research Laboratories, West Point, PA 19486 2002-2005: Graduate Research Assistant, Dept of Biomedical Sciences, University of Missouri-Columbia, MO 65211 2001: Intern Veterinarian, Veterinary Poly Clinic, Kurnool, AP, India-518001 DETAILED RESPONSIBILITIES: Fields of experience: Oncology/Cardiovascular/Diabetes/Neurology/Endocrine/Immunology 2008-2010: Translational Scientist, Huntingdon Life Sciences: This customer focused position acted as a “Scientific Liaison” for biomarker selection and analysis by providing strong scientific link between clients and analytical departments at Huntingdon Life Sciences’ UK and US facilities. Preclinical and clinical biomarker analyses were undertaken by genomics, MRI-PET tracers, Veridex (circulating tumour cells) CTCs, immunoassay, LC-MS, histopathology, mass spectrometry, and cell based assays. Job Responsibilities: Biomarker advisory services: • Play a pivotal role as a Preclinical and Clinical R&D advisor (GLP/GCP) in recommending biomarker/personalized medicine (diagnostics) strategies and applications based on sponsor's small molecule/biologics drug development programs. • Translating scientific or clinical data into high quality medical information to help clinical investigators best design their drug development programs. 1
  • 2. Dr. Kamala Kalyani Maddali DVM, PhD • Responsible for the creation and ownership of a biomarker work plan (for clinical protocols) for clinical and preclinical phases by interacting with healthcare professionals/pharmaceutical investigators/physicians etc. • Project management with Pharma/biotech clients to best understand client project objectives and goals • Implement pricing/new technology strategies globally with in the company • Scientifically translate client needs into effective research plan • Execute research plan as part of a team including survey design, data analysis, and structuring of presentations and also responsible for professional review of the published literature as well as other sources of information to provide team members with timely summaries and critical evaluations of advances in basic and clinical programs. Business Development activities: Act as a “consultant” in the following activities: • Establish and maintains effective communication/coordination with sponsors, field sales, and managed market account representatives. Traveling to client sites and interacting with sponsors on a regular basis through communications, publication planning, slide decks, manuscript publications and marketing case studies • Works closely with the global director of marketing/sales in regard to biomarkers/personalized medicine on the management of diverse R and D programs. • Stays abreast with literature in the field and contributes to case studies, pricing strategies, forecasting markets, proposal writing, and other strategic development efforts. • Identifies, interacts and maintains relationships with consultants, vendors and KOLs in the arena of biomarkers/personalized medicine field involving pharmaceutical/biopharmaceutical clients. • Represented HLS at several national scientific meetings (ASCO, DIA, SOT etc.). Business development through customized presentations and creating distinctive marketing materials for HLS Biomarker services. • Matrix involvement with four “Analytical groups” with 6 PhD’s involving Flow cytometry/Immunoassay/Clinical Pathology/Mass Spec/Histopathology/Immunohistochemistry. Process Improvements: • Create a Business Biomarker Proposal Process for initial communication with the clients and a hand-off of the project to Operations group. • Create a formal feedback mechanism for client communication and measurement of client satisfaction by initiating monthly "Process Improvement" meetings between Operations and Business Development. 2005-2008: Research Associate, Merck Research Laboratories 1. Development of in vivo pharmacology and toxicity models that can be used to screen drug development candidates; leading to go/no-go decisions. Work with researchers on study designs during lead optimization of the drug development process. Experience working in the area of cancer (knock-out mice models), metabolic disorders (diabetes, obesity, atherosclerosis), cardiovascular, inflammatory diseases. 2
  • 3. Dr. Kamala Kalyani Maddali DVM, PhD 2. Formulate and execute novel strategies to decrease attrition of drug development candidates due to toxicity. 3. Plan experimental approaches (GLP/Non-GLP) to gain mechanistic understanding around safety signals observed in preclinical toxicity studies and place in context of human risk. 4. Develop translatable biomarkers to effectively monitor and manage safety in humans. 5. Identify the key routes to translate in vitro observations into whole animal studies to provide in vivo Proof of Concept/ Proof of Mechanism for novel therapeutic candidates. 6. Identify efficacy markers (“biomarkers”) in animal models (oncology/endocrine/cardiovascular) which may be translatable into human studies and ensure that these are appropriately examined in translational approaches. 7. Dotted line supervision of a laboratory (with 4-5 scientific staff) for biomarkers (Molecular Diag- nostics Lab) and training technical staff in newly introduced techniques (through IHC/RT-PCR/Lu- minex/Meso-scale/Veridex (CTCs); etc). Interactions with local lab leads & scientists from Discov- ery and Safety Assessment groups. 8. Key role in the oncology, inflammatory and myotox biomarker committees tasked with the identifi- cation and validation of safety biomarkers. 9. Translational animal model experience working in the area of oncology, neuroscience, metabolic disorders (diabetes, obesity, atherosclerosis), cardiovascular, endocrine disorders, inflammation, hypertension. a. Oncology models b. Neuroscience models-Alzhimers/Parkinsons/Sleep Apnea c. Cardiovascular models- Atherosclerosis/Restenosis models d. Obesity models – Primates- Rhesus, Cynologous Monkeys; Rats, Mice, Marmosets e. Respiratory models-Cough model f. Inflammatory models. 10. Development, validation, and implementation of technologies that include: a. Veridex/CTC b. MRI/PET c. FLIPR d. MSD/Luminex e. Flow Cytometry f. LC-MS g. Confocal microscopy h. Electron microscopy i. RT-PCR j. Immunoprecipitation k. Immunohistochemistry l. Laser Capture Micro dissection m. Western Blots 2002-2005: Graduate Research Assistant, University of Missouri-Columbia, MO 65211 Thesis Title: A Mandatory requirement of PKC-delta in testosterone regulated smooth muscle cell differentiation, proliferation, and apoptosis • Training in porcine and rat models of atherosclerosis and restenosis 3
  • 4. Dr. Kamala Kalyani Maddali DVM, PhD • Investigated the role of inflammation and protein trafficking in coronary heart disease utilizing in vivo and ex-vivo porcine models and cell based assays • Delineating the role of various cell cycle proteins (positive and negative cell cycle regulators), ap- optotic proteins, signalling pathways like PKC, MAP kinase, and lipid and lipoprotein metabolism in the regression of coronary plaques in porcine disease models. • 4 year extensive training in various in vivo and in vitro techniques such as primary cell cultures, western blots, flow cytometry, confocal microscopy, siRNA based gene knockouts, immunohisto- chemistry etc. 2001: Intern Research Veterinarian, Veterinary Poly Clinic, Kurnool, AP, India-518001 GRANTS AND AWARDS: 2005: American Heart Association Heartland Affiliate: $ 50,000 Grant Title: “Testosterone Regulation of Coronary Smooth Muscle Cell Differentiation and Proliferation” PUBLICATIONS AND PRESENTATIONS:  K.K. Maddali- “Invited speaker for Association of Inhalation Toxicology, Germany-Biomarkers in COPD”, October 2010.  K.K. Maddali- “Invited speaker for AECCP, Verona, Italy-Translational strategies for cardiac biomarkers”, Sep 2010.  K.K.Maddali, Sample processing and Biomarker analysis”. Webinar for ACRP, 2009.  K.K. Maddali- “It is time to implement an early renal toxicity biomarker strategy”, Developments in Life Sciences (HLS internal journal), Vol. 9, No. 1.  K. K. Maddali, C. I. Starks, C. McDonough, J. Dharmadhikari, B. A. Litzenberger Bone biomarkers significantly enhances the predictability of preclinical study outcomes and translation to first in man studies targeted towards osteoporosis. AACC National Meeting, 2009.  KK Maddali, IT Rogers, SL Motzel D Connor H Klein Development of Cough model in Guinea Pigs National AALAS, Charlotte, NC 2007.  KK Maddali, IT Rogers, SL Motzel D Connor, H Klein Development and validation of Biomarkers in Rhesus monkey model of Diet induced obesity, ENDO, Canada, 2007.  D. K. Bowles, K. K. Maddali, V. C. Dhulipala, and D. H. Korzick PKC-delta mediates anti- proliferative, pro-apoptic effects of testosterone on coronary smooth muscle. Am J Physiol Cell Physiol, August 2007; 293(2): C805 - C813.  KK Maddali, IT Rogers, SL Motzel D Connor, H Klein Metabalonomic markers in obesity monkey models, ENDO, San Diego, 2006.  KK Maddali, DH Korzick, JR Turk and DK Bowles. Isoform-specific modulation of coronary PKC by glucocorticoids. Vascular Pharmacology. 2005 42:153-162.  KK Maddali, DH Korzick, Tharp DL and DK Bowles. PKC-delta mediates testosterone-induced increases in coronary smooth muscle Cav1.2. J Biol Chem. 2005 Dec 30;280(52):43024-9. Epub 2005 Oct 21.  KK Maddali, Donna Korzick and Douglas K. Bowles. Testosterone alters coronary proliferation through PKC-delta mediated mechanism. Experimental Biology, 2005. FASEB J.  KK Maddali, Donna Korzick and Douglas K. Bowles. Testosterone alters coronary apoptosis through PKC-i , delta mediated mechanism. Experimental Biology, 2005. FASEB J.  Vamsidhara C. Dhulipala, KK Maddali, Wade V. Welshons and Chada S. Reddy. Effects of Secalonic acid-D toxin, on murine palatal mesenchymal cell cycle. Developmental and Reproductive Toxicology, Birth defects Journal, 2005, June ;74(3):233-42.  Bowles DK, Cl Heaps, JR Turk, KK Maddali, EM Price. Hypercholesterolemia inhibits L-type calcium channel current in coronary macro-, not micro circulation. Journal of Applied Physiology, 2004 June; 96(6):2240-8.  Bowles DK, KK Maddali, VK Ganjam, LJ Rubin, DL Tharp and CL Heaps. Endogenous testosterone increases L-type Ca2+ channel expression in porcine coronary smooth muscle. American Journal of Physiology – Heart and Circulatory Physiology, 2004 Nov; 287(5):H2091-8. 4
  • 5. Dr. Kamala Kalyani Maddali DVM, PhD  KK Maddali, Donna Korzick and Douglas K. Bowles. Testosterone alters coronary PKC- delta expression and PKC-mediated Voltage gated calcium channel expression, 6587, Experimental Biology, 2004.  KK Maddali, Donna Korzick and Douglas K. Bowles. Effect of glucocorticoids on PKC isoform expression in porcine coronary arteries, 6330, Experimental Biology, 2003. REFERENCES: Provided upon request 5