Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

7.8%

5 terminated/withdrawn out of 64 trials

Success Rate

91.2%

+4.7% vs industry average

Late-Stage Pipeline

23%

15 trials in Phase 3/4

Results Transparency

62%

32 of 52 completed trials have results

Key Signals

32 with results

Enrollment Performance

Analytics

Phase 1
23(44.2%)
Phase 2
14(26.9%)
Phase 3
10(19.2%)
Phase 4
5(9.6%)
52Total
Phase 1(23)
Phase 2(14)
Phase 3(10)
Phase 4(5)

Activity Timeline

Global Presence

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Clinical Trials (64)

Showing 20 of 64 trials
NCT03877926Phase 3Completed

VELOCITY: An Anthrax Vaccine Clinical Study

Role: lead

NCT05377255Phase 1Completed

Pharmacokinetics (PK) and Safety of Multiple Doses of Intranasal Naloxone in Healthy Adults

Role: lead

NCT07478471Not Yet Recruiting

Observational Study of Raxibacumab in Sporadic Cases of Systemic Anthrax

Role: lead

NCT03569553Not Yet Recruiting

A Field Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in Inhalational Anthrax Patients

Role: lead

NCT03569514Not Yet Recruiting

Observational Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in Patients With Systemic Anthrax

Role: lead

NCT02177721Phase 4Not Yet Recruiting

Clinical Benefit and Safety of Raxibacumab in Patients With Symptomatic Inhalational Anthrax in a Mass Exposure Scenario

Role: lead

NCT02051062Phase 4Enrolling By Invitation

BT-011 Pharmacokinetics of Botulism Antitoxin Heptavalent in Pediatric Patients

Role: lead

NCT07268612Not Yet Recruiting

Evaluation of Clinical Benefit and Safety Following CYFENDUS Administration for Post-Exposure Prophylaxis of Anthrax Disease.

Role: lead

NCT01374984Enrolling By Invitation

VA-005 Clinical Outcomes of VIGIV Treatment of Smallpox Vaccination Complications or Vaccinia Infection

Role: lead

NCT04067011Phase 2Completed

Velocity 2: An Anthrax Vaccine and Antibiotics Clinical Study

Role: lead

NCT01753115Phase 2Completed

Ciprofloxacin BioThrax Co-Administration Study

Role: lead

NCT05142306Phase 1Completed

A COVID-19 Study to Evaluate Safety and PK of COVID-HIG Administered Through IM, SC, or IV Routes to SARS-CoV-2 Uninfected Adults

Role: lead

NCT04661839Phase 1Completed

A COVID-19 Study to Evaluate Safety and Pharmacokinetics of COVID-HIGIV Administered in Healthy Adults

Role: lead

NCT05194358Phase 1Completed

Study of SIAN Nasal Spray in Healthy Adults

Role: lead

NCT05155319Phase 1Completed

Universal Influenza A Vaccine in Healthy Adults

Role: lead

NCT05935917Phase 1Completed

Study Evaluating the Bioequivalence of Brincidofovir Form H and Form II Tablets in Healthy Adults

Role: lead

NCT05349617Phase 3Completed

Safety and Immunogenicity of CHIKV VLP Vaccine PXVX0317 in Adults ≥65 Years

Role: collaborator

NCT03992872Phase 2Completed

Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317)

Role: collaborator

NCT05072080Phase 3Completed

A Phase 3 Trial of the VLP-Based Chikungunya Vaccine PXVX0317 (CHIKV VLP Vaccine)

Role: collaborator

NCT00679172Phase 2Completed

Immunogenicity, Safety and Tolerability of the Typhoid Fever Vaccine Candidate M01ZH09 in Healthy Adults

Role: lead