Cholera
Pipeline by Development Stage
Drug Modality Breakdown
On Market (1)
Approved therapies currently available
Competitive Landscape
10 companies ranked by most advanced pipeline stage
Trial Timeline
Clinical trial activity over time
Showing 15 of 18 trials with date data
Clinical Trials (18)
Total enrollment: 90,749 patients across 18 trials
To Evaluate Safety of Oral Cholera Vaccine Hillchol® (BBV131)
A Phase III Randomized, Modified Double-blind, Multi-centric, Comparative Study, to Evaluate the Non-inferiority of Immunogenicity and Safety of Hillchol® (BBV131)to Shanchol™ Along With Lot-to-lot Consistency of Hillchol®(BBV131).
Immune Non-Inferiority, Safety and Lot-to-Lot Consistency of Oral Cholera Vaccine-Simplified Compared to Shanchol™
Safety and Immunogenicity of a New Formulation of Euvichol®
A Study of Live Oral Cholera Vaccine, PXVX200 in Healthy Older Adults
A Phase 3 Lot to Lot Consistency Study of Live Oral Cholera Vaccine, PXVX0200 in Healthy Adults
Safety and Efficacy Challenge Study of Live Oral Cholera Vaccine Candidate,PXVX0200, to Prevent Cholera
Single Dose Ciprofloxacin in the Treatment of Childhood Cholera:Randomized Controlled Clinical Trial
Cholera Anti-Secretory Treatment Trial
Immunologic Responses to a Live Attenuated Oral Cholera Vaccine
PXVX0200 (CVD103-HgR) vs Shanchol in Mali
Safety and Immunogenicity of Locally Manufactured New (HL-OCV) Oral Cholera Vaccine
Safety and Immunogenicity of the Live Oral Cholera Vaccine Candidate PXVX0200
Cholera-Hospital-Based-Intervention-for-7-Days (CHoBI7) Water, Sanitation, and Hygiene (WASH) Case Area Targeted Intervention (CATI)
Water, Sanitation, and Hygiene Mobile Health Messages as an Innovative Tool to Facilitate Behavior Change
Cholera Vaccine Investment Strategy in Bangladesh
Protective Immunity to Human Cholera in Bangladesh
Immunity to Human Cholera in Bangladesh
Phase Legend
Key Insights
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.