Autopsy report · NCT02125266
Safety and Preliminary Efficacy Study of V404 PDS in Uveitis
Cause of deathSafety
“Study terminated due to unacceptable frequency of drug related adverse events”
Life of this trial
- Ran for about 11 months before it stopped.
- 7 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Forsight Vision4
- Sponsor type
- Industry
- Conditions
- Uveitis, Posterior; Uveitis, Intermediate
- Interventions
- V404
- Participants
- 7
- Sites
- 5
- Countries
- United States
Trials that died the same way
- Panobinostat/Velcade in Multiple Myeloma
“This study was terminated because the drug company stopped making the study drug” - Phase II Study of Aldesleukin (IL-2) Following the Administration of Zanolimumab (Anti-CD4mAb) in Metastatic Melanoma and Metastatic Renal Cancer
“The study was terminated because we were not able to obtain the study drug.” - Safety Study of Bevacizumab (Avastin) With Thoracic Radiation in Non-small Cell Cell Lung Cancer
“Study terminated due to toxicity” - One Year Study of Rifaximin Delayed Release (DR) in Crohn's Disease
“The study was terminated early due to difficulty in enrollment and lack of clinical study drug access.” - Phase II Study of TPA Plus Dexamethasone & CMT in Hematologic Malignancies
“Study was terminated early due to lack of experimental medication (supply issues)”
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.