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NCT02664961 · ClinicalTrials.gov registry record · Phase 2

Study of TRC105 and Bevacizumab in Patients With Refractory Gestational Trophoblastic Neoplasia (GTN)

A Phase 2 study, sponsored by Tracon Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
3
Enrollment target

NCT02664961: Clinical Trial Phase 2 study, sponsored by Tracon Pharmaceuticals.

NCT02664961 is a Phase 2 study that was terminated before completion, run by Tracon Pharmaceuticals. The registered enrollment target is 3 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02664961, a Phase 2 study, was terminated before completion, sponsored by Tracon Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
3 participants
Enrollment target

Study Summary

The purpose of the study is to determine the overall response rate of single agent TRC105 and the combination of TRC105 and bevacizumab in patients with refractory GTN (including choriocarcinoma, placental site trophoblastic tumor (PSTT), and epithelioid trophoblastic tumor (ETT)). Up to 30 patients will be treated.

Primary Outcome

Antitumor Activity of Single Agent TRC105 and the Combination of TRC105 and Bevacizumab will be assessed via RECIST 1.1 and by measuring circulating bHCG. Disease progression is defined as \>20% increase (the absolute increase must be ≥10 IU/L) above the nadir on consecutive measurements separated by at least two weeks; Partial response is defined as a hCG decrease of 50% or more from starting value on consecutive measurements; Complete response will be defined as normalization of hCG on consecu

Interventions

  • DRUG Bevacizumab
  • DRUG TRC105

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2016-03
Est. Completion 2018-11
Phase Phase 2
Tracon Pharmaceuticals

16 total trials

Why NCT02664961 stopped before completion

NCT02664961 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower).

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

NCT02664961 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02664961 about?

NCT02664961 is a clinical study titled "Study of TRC105 and Bevacizumab in Patients With Refractory Gestational Trophoblastic Neoplasia (GTN)". The purpose of the study is to determine the overall response rate of single agent TRC105 and the combination of TRC105 and bevacizumab in patients with refractory GTN (including choriocarcinoma, placental site trophoblastic tumor (PSTT), and epithelioid trophoblastic tumor (ETT)). Up to 30 patients...

What is the current status of trial NCT02664961?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 3 participants. The study started on 2016-03. Estimated completion is 2018-11.

What interventions are being tested in trial NCT02664961?

The interventions under investigation include: Bevacizumab (DRUG), TRC105 (DRUG).

Who is sponsoring clinical trial NCT02664961?

This trial is sponsored by Tracon Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02664961's enrollment target sits among peer trials

3 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02664961, the US trial registry maintained by the National Library of Medicine. NCT02664961 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.