Autopsy report · NCT04807972
Study to Evaluate Adverse Events and Change in Disease Activity When Intravenous (IV) Infusion of ABBV-927 is Administered in Combination With IV Modified FOLFIRINOX (mFFX) With or Without IV Budigalimab Compared to mFFX in Adult Participants With Untreated Pancreatic Cancer Metastasis
Cause of deathFunding or business
“Strategic considerations”
Life of this trial
- Registered 2 months before it started.
- Ran for about 2 years 10 months before it stopped.
- 40 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- AbbVie
- Sponsor type
- Industry
- Conditions
- Pancreatic Cancer
- Interventions
- ABBV-927; Budiglimab; modified FOLFIRINOX
- Participants
- 40
- Sites
- 15
- Countries
- Australia, Israel, Puerto Rico, South Korea, Spain, United States
Trials that died the same way
- CT 327 in the "Atopy Patch Test" Model
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“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.