3. What Is AMR?
Antimicrobial resistance (AMR) is the ability of
microorganisms that cause disease to withstand
attack by antimicrobial medicines
AMR is rapidly becoming a major
public health risk and is threatening
to undo decades of advances in
treating disease
4. Increased use of antibiotics
Prescriptions taken incorrectly
Sold without medical supervision
Prophylactic use before surgery
Antibiotics used for viral infection
Spread of resistant microbes in hospitals due to lack of hygiene
Patients who do not complete course
Antibiotics in animal feeds
What Has Led To Resistance?
5. Methods of Resistance
Impermeability of the drug
Alteration in the drug’s target
Enzymatic drug modification
Efflux of the drug
Methods of Resistance Acquisition
Chromosomal mutation
Genetic transfer (ex: plasmids)
Mechanisms Of Resistance: Overview
6. Superbug Statistics
Death From Drug-Resistance Infection Set To Skyrocket
Deaths from antimicrobial resistant infections and other causes in 2050
Antimicrobial resistant
infections
10.0 m
Cancer 8.2m
Diabetes 1.5m
Diarrhoeal Disease 1.4
Road traffic accident 1.2m
Measles 130,000
Cholera 120,000
7. The latest investment stats from CARB-X
Pharmaceutical Companies and the Superbugs War
0
5
10
15
20
25
30
27 22 09 16 14 08 22 12
Large Research Based Pharmaceutical Companies.
0
5
10
15
20
7 17 7 10 4 10 11 6
7 11 11 10
Pharmaceutical and biopharmaceutical companies leading the charge against superbugs
Bio Pharmaceutical Companies.
3
8
21
9
16
12
8
13
13 13
3
13
5
16
10
9 9 9
10
14
R & D
Remaining potential score
Money For The War On Superbugs
8. Rethink The Way Fighting Bugs:
WHO WE ARE?
A strong inter-disciplinary team of 150 scientists.
WHAT WE DO?
We aim to provide effective, safe and robust treatment that target Gram-
negative bacteria ,especially the bacteria involved in nosocomial and urinary
tract infection.
9. Gram-Negative Bacterial Infections
Massive Urgent GLOBAL Unmet Need
Causes many life-threatening illnesses
Pneumonia, Sepsis, complicated urinary tract infections, post-surgical
intra-abdominal infections, burn injury infections etc.
Key Culprits
Pseudomonas aeruginosa, Acinetobacter baumannii, Klebsiella
pneumoniae, Escherichia coli, Enterobacter spp. etc.
No new Gram-negative antibiotic since 1962
WHY: Extremely Well Protected
Permeability barriers for entry
Multiple Efflux Pumps
Focus Area
10. Our Technologies:
1. Developing new molecules or derivatives of existing antibiotics with same or
different MoA:
Super Bugs Need Drugs
Entry into Phase 1 clinical trials
Preclinical development
Candidate Declartion
Drug delivery,
extensive in vivo
efficacy profiling
12. Stabicon’s Initiative On Anti Microbial Resistance
11 formulations developed and analyzed
Two(2) positive potential
̶ Greater solubility
̶ Effective in by passing fast pass metabolism
̶ Improved targeted delivery
̶ Boost up immunity