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NCT01940172 · ClinicalTrials.gov registry record · Phase 1

Study of Birinapant in Combination With Conatumumab in Subjects With Relapsed Ovarian Cancer

A Phase 1 study, sponsored by TetraLogic Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
27
Enrollment target

NCT01940172: Completed Phase 1 study, sponsored by TetraLogic Pharmaceuticals.

NCT01940172 is a Phase 1 study that has completed, run by TetraLogic Pharmaceuticals. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01940172, a Phase 1 study, has completed, sponsored by TetraLogic Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

This is a dose escalation study in female subjects with relapsed ovarian cancer (including epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer). Approximately 30 to 40 subjects will be administered a combination of conatumumab and birinapant. In the initial dose-escalation stage of the study, adult female subjects will receive conatumumab in combination with increasing doses of birinapant in dose-escalation cohorts to determine the MTD of birinapant when administered with a fixed dose of conatumumab. In safety expansion stage, adult female subjects will receive conatumumab in combination with birinapant at the MTD of the combination.

Interventions

  • DRUG Birinapant
  • DRUG Conatumumab

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2013-11
Est. Completion 2015-12
Phase Phase 1
TetraLogic Pharmaceuticals

6 total trials

What the finished NCT01940172 record still lists

NCT01940172 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

The record links to 0 conditions, and to 2 interventions - of which Birinapant is the first listed.

NCT01940172 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01940172 about?

NCT01940172 is a clinical study titled "Study of Birinapant in Combination With Conatumumab in Subjects With Relapsed Ovarian Cancer". This is a dose escalation study in female subjects with relapsed ovarian cancer (including epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer). Approximately 30 to 40 subjects will be administered a combination of conatumumab and birinapant. In the initial dose-escalatio...

What is the current status of trial NCT01940172?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2013-11. Estimated completion is 2015-12.

What interventions are being tested in trial NCT01940172?

The interventions under investigation include: Birinapant (DRUG), Conatumumab (DRUG).

Who is sponsoring clinical trial NCT01940172?

This trial is sponsored by TetraLogic Pharmaceuticals, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01940172's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01940172, the US trial registry maintained by the National Library of Medicine. NCT01940172 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.