Autopsy report · NCT03400306
A Study Evaluating the Bioavailability and Food Effect of Veliparib Tablets Followed by an Extension in Subjects With Ovarian Cancer
Cause of deathFunding or business
“Strategic considerations”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 1
- Sponsor
- AbbVie
- Sponsor type
- Industry
- Conditions
- Cancer - Ovarian
- Interventions
- Veliparib, capsule; Veliparib, tablet; Carboplatin; Paclitaxel
- Participants
- 0
Trials that died the same way
- CD8 Minibody Repeatability Study
“Strategic decision” - Evaluation of the Safety, Tolerability, and Efficacy of MDGN-002 in Adults With Moderate to Severe Active Crohn's Disease or Ulcerative Colitis
“Strategic reasons” - Rapid Amniotic Fluid (AF) Test and a Non-Invasive Vaginal Fluid (VF) Test
“Business Strategic Decision” - Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis
“Strategic business decision” - S095033 in Combination With Paclitaxel as 2nd- or 3rd-line Treatment in Participants With Advanced or Metastatic ESCC
“Strategic development reasons”
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.