Anthrax clinical trials
The registry lists 75 studies for Anthrax across more than 10 countries. 12 are recruiting or about to start. 58 of them are mainly about Anthrax (how this is decided). Per ClinicalTrials.gov, last updated 2026-10-20.
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Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
Now Active, not recruiting
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Who runs them
Emergent BioSolutions (14) · National Institute of Allergy and Infectious Diseases (NIAID) (7) · Elusys Therapeutics (4) · Bayer (3) · PharmAthene, Inc. (3) · Biomedical Advanced Research and Development Authority (2) · Taichung Veterans General Hospital (2) · Centre Hospitalier Universitaire de Saint Etienne (2)
What is being tested here
Drugs under test in Anthrax studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
| Drug | Open | Phase 3 | All |
|---|---|---|---|
| Charcoal | 2 | 0 | 8 |
| Obiltoxaximab | 1 | 0 | 5 |
| Canagliflozin | 1 | 0 | 1 |
| AV7909 | 0 | 1 | 7 |
| Biothrax | 0 | 1 | 5 |
| MDX-1303 | 0 | 0 | 3 |
| Ciprofloxacin | 0 | 0 | 2 |
| Rivaroxaban | 0 | 0 | 2 |
| Doxycycline | 0 | 0 | 1 |
| Glyburide | 0 | 0 | 1 |
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 3
- Jul 2027Observational Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in Patients With Systemic Anthrax · Emergent BioSolutions
- Jul 2027A Field Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in Inhalational Anthrax Patients · Emergent BioSolutions
- Oct 2027SGLT2 Inhibitor Utilization Re-perfusion Therapy · Taichung Veterans General Hospital
Who these studies take
Of the 4 Anthrax studies recruiting now, 4 (100%) set no upper age limit and 0 (0%) stop at 75 or younger. 1 (25%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 0 (0%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 1 (25%) | 1 (25%) |
| 18 | 3 (75%) | 3 (75%) |
| 30 | 4 (100%) | 4 (100%) |
| 40 | 4 (100%) | 4 (100%) |
| 50 | 4 (100%) | 4 (100%) |
| 65 | 4 (100%) | 4 (100%) |
| 75 | 4 (100%) | 4 (100%) |
| 85 | 4 (100%) | 4 (100%) |
Across all 75 studies, recruiting or not: 57% stop at 75 or younger and 56% at 65; 23% take children; 0% are for women only and 5% for men only; 63% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
How long Anthrax studies take
Of 11 phase 1 interventional studies under Anthrax, half reached primary completion within 14 months of starting, counting those still running.
| Start to primary completion | Every sponsor | Industry | Non-industry |
|---|---|---|---|
| Phase 1 | 14 mo8–18 · 11 studies | — | — |
Each figure is the month by which half the studies had reached primary completion, with the range in which the middle half did. Studies still running count until their last registry update; studies that stopped early are left out. Phase 1 includes early phase 1; observational means prospective or not stated, as retrospective and cross-sectional studies date a window of data rather than a study. How these figures are worked out
Studies
Recruiting first, then most recently updated. Showing 50 of 75. Browse all 75 → or search them.
- Combined Gastrointestinal Decontamination in Acute Severe PoisoningRecruitingNCT07201311Phase 21 country
- Cigarette Filter StudyRecruitingNCT07348679Not applicable1 country
- SGLT2 Inhibitor Utilization Re-perfusion TherapyNot yet recruitingNCT06858436Phase 4
- Observational Study of Raxibacumab in Sporadic Cases of Systemic AnthraxNot yet recruitingNCT07478471
- Clinical Benefit and Safety of Raxibacumab in Patients With Symptomatic Inhalational Anthrax in a Mass Exposure ScenarioNot yet recruitingNCT02177721Phase 4
- Observational Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in Patients With Systemic AnthraxNot yet recruitingNCT03569514
- A Field Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in Inhalational Anthrax PatientsNot yet recruitingNCT03569553
- Activated CHARcoal in Poisoned Patient - Pilot TrialRecruitingNCT05471479Phase 41 country
- Evaluation of Clinical Benefit and Safety Following CYFENDUS Administration for Post-Exposure Prophylaxis of Anthrax Disease.Not yet recruitingNCT07268612
- The Effect of Probiotics vs Activated Charcoal in the Management of CKD Patients Suffering From Uremic Pruritus.Not yet recruitingNCT06579066Phase 2
- A Case-control Study on the Clinical Characteristics of 28-day and 90-day Death From Severe AnthraxRecruitingNCT063650731 country
- An Open Label Field Study of Anthim (Obiltoxaximab) in Subjects Exposed to B. AnthracisNot yet recruitingNCT03088111Phase 4
- Anthrax AV7909 Boost Evaluation StudyCompletedNCT05997264Phase 21 country
- Natural History of Anthrax: a Study of Primary Infected, Recovered, and Exposed Individuals (SPoRE); and Evaluation of AVA-Vaccinated RecipientsCompletedNCT000503101 country
- Effect of Activated Charcoal on Serum Osmolality, Osmolal Gap, and Enzymatic Ethylene Glycol AssayActive, not recruitingNCT072200311 country
- The Effect of AC-134 in Chronic Kidney DiseasesCompletedNCT06441435Not applicable1 country
- VELOCITY: An Anthrax Vaccine Clinical StudyCompletedNCT03877926Phase 31 country
- Comparative Clinical Assessment of Charcoal and Conventional ToothbrushesCompletedNCT07563413Not applicable1 country
- Activates Charcoal for Patients Undergoing Invasive Procedure Delayed Due to Direct Oral AnticoagulantsWithdrawnNCT02969746Phase 41 country
- Velocity 2: An Anthrax Vaccine and Antibiotics Clinical StudyCompletedNCT04067011Phase 21 country
- NasoShield in Healthy Adults to Study Safety and ImmunogenicityCompletedNCT04415749Phase 11 country
- NasoShield Study of Safety and ImmunogenicityCompletedNCT03352466Phase 11 country
- Ciprofloxacin BioThrax Co-Administration StudyCompletedNCT01753115Phase 21 country
- Anthrax AV7909 Liquid vs LyophilizedCompletedNCT04660201Phase 11 country
- Glyburide Advantage in Malignant Edema and Stroke - Remedy PharmaceuticalsCompletedNCT01794182Phase 21 country
- Anthrax Vaccine Clinical Trial to Assess Dose Reduction and Route ChangeCompletedNCT00119067Phase 41 country
- Immunogenicity and Safety Study of a Three-Dose BioThrax® Regimen for Post-Exposure Prophylaxis in Healthy AdultsCompletedNCT01491607Phase 31 country
- Safety, Tolerability and Immunogenicity Study of AV7909 Anthrax Vaccine in Healthy AdultsCompletedNCT01263691Phase 11 country
- A Phase 1 Ascending Dose Study to Assess the Safety and Immunogenicity of Adenovirus Anthrax Vector Candidate VaccinesCompletedNCT01979406Phase 11 country
- Safety and Pharmacokinetics Study of Anthrax Immune Globulin Intravenous (AIGIV)CompletedNCT00845650Phase 1/21 country
- A Phase 2 Safety and Immunogenicity Study for an Anthrax Vaccine Using 3 Schedules and Two Dose LevelsCompletedNCT01770743Phase 21 country
- Safety and Pharmacokinetics Study of Human Monoclonal Antibody (AVP-21D9)CompletedNCT01202695Phase 11 country
- Evaluation of the SRI B. Anthracis Lethal Factor Diagnostic SystemTerminatedNCT056728751 country
- A Pilot Feasibility Study of Activated Charcoal in Healthy VolunteersCompletedNCT04204772Early Phase 11 country
- A Study to Assess Dose-Response, Efficacy (Immunogenicity) and the Safety of GC1109CompletedNCT01624532Phase 21 country
- Non Inferiority Study of a Reduced Dose of Activated Charcoal on Rivaroxaban Pharmacokinetics.CompletedNCT04767776Phase 11 country
- A Study to Evaluate the Effect of Activated Charcoal With Sorbitol on the Single-dose of Mavacamten in Healthy ParticipantsCompletedNCT05320094Phase 11 country
- Effects of CharcoCaps® (Activated Charcoal) vs. Placebo on Intestinal Gas ProductionCompletedNCT05510778Not applicable1 country
- A Safety and Immunogenicity of Intranasal Nanoemulsion Adjuvanted Recombinant Anthrax Vaccine in Healthy AdultsCompletedNCT04148118Phase 11 country
- Charcoal in Lung Cancer Patients Undergoing TEMLAWithdrawnNCT04928950Phase 2
- Evaluation of the Clinical Specificity of the Active Anthrax Detect™ Plus (AAD Plus) Lateral Flow Immunoassay (LFI)CompletedNCT043204851 country
- Foster With or Without Charcoal Block or Aerochamber PlusCompletedNCT01280175Phase 11 country
- BARDA Securing Anthrax Immunity For the ElderlyCompletedNCT03518125Phase 21 country
- Special Drug Use Investigation of Ciproxan Injection in PediatricsCompletedNCT025550591 country
- EPR Tumor Oximetry With CE India InkTerminatedNCT033219031 country
- Safety, Tolerability and PK of Repeat Administration of Intravenous ETI-204 in Adult VolunteersCompletedNCT01932242Phase 11 country
- Safety, Tolerability, and PK of a Single Intravenous Dose of ETI-204 in Adult VolunteersCompletedNCT01929226Phase 11 country
- Febrile Whole Blood Specimen Collection and TestingCompletedNCT034980271 country
- An Open-label, Nonrandomized Study to Evaluate the Safety and Immunogenicity of Raxibacumab With ReinjectionCompletedNCT02016963Phase 2/3
- A Phase I Study of Safety and Immunogenicity of the WRAIR HIV-1 VaccineCompletedNCT00412477Phase 11 country