Autopsy report · NCT01740388
Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis
Cause of deathFunding or business
“Strategic business decision”
Life of this trial
- Registered 3 months before it started.
- Ran for about 9 months before it stopped.
- 136 participants enrolled.
- Results were posted on the registry 10 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Bausch & Lomb Incorporated
- Sponsor type
- Industry
- Conditions
- Bacterial Conjunctivitis
- Interventions
- Besifloxacin; Vehicle
- Participants
- 136
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Rapid Amniotic Fluid (AF) Test and a Non-Invasive Vaginal Fluid (VF) Test
“Business Strategic Decision” - CD8 Minibody Repeatability Study
“Strategic decision” - Dendritic Cell Immunotherapy Plus Standard Treatment of Advanced Renal Cell Carcinoma
“Strategic corporate decision” - A Study to Evaluate the Effects of ASP5502 in Healthy Adults and Adults With Primary Sjögren's Syndrome
“Company's strategic decision” - A Study of RBI-4000 in Healthy Participants
“Strategic business decision (not related to safety, efficacy, or quality)”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.