Autopsy report · NCT02577029
Study of ARC-520 With or Without Other Drugs Used in the Treatment of Chronic Chronic Hepatitis B Virus (HBV)
Cause of deathFunding or business
“Company decision to discontinue trial”
Life of this trial
- Registered 2 months before it started.
- Ran for about 1 year before it stopped.
- 79 participants enrolled.
- Results were posted on the registry 2 years 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Arrowhead Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Hepatitis B; Hepatitis D
- Interventions
- ARC-520; entecavir; pegylated interferon alpha 2a; tenofovir disoproxil; antihistamine
- Participants
- 79
- Sites
- 33
- Countries
- Australia, Bulgaria, China, Moldova, New Zealand, South Korea, Taiwan, Thailand
Trials that died the same way
- One Touch® Verio®IQ European Clinical Outcomes Study
“Business decision to withdraw trial” - A Safety and Tolerability Study of Doripenem Compared With Cefepime in Hospitalized Children With Bacterial Pneumonia
“Trial terminated early per business decision” - Study of Inlexisertib (DCC-3116) in Participants With RAS/MAPK Pathway Mutant Solid Tumors
“Trial terminated due to business decision, not based on any safety or efficacy concerns.” - Regorafenib-pembrolizumab vs. TACE/TARE in Intermediate Stage HCC Beyond Up-to-7
“The trial ended earlier than planned due to slow enrolment, which has made it unfeasible to achieve the target sample size within a reasonable timeframe. Consequently, a business decision has been made to discontinue funding for the trial.” - A Study to Learn About the Effect of Avelumab First-Line Maintenance in Canadian People With Advanced Bladder Cancer
“The trial was terminated for strategic reasons. The decision was not based on any safety and/or efficacy concerns.”
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.