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NCT02396511 · ClinicalTrials.gov registry record · Phase 2

TRC105 Combined With Standard-dose Bevacizumab for Two Patients With Metastatic And Refractory Choriocarcinoma

A Phase 2 study of Choriocarcinoma, sponsored by Tracon Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
2
Enrollment target
1
Study location

NCT02396511: Completed Phase 2 study of Choriocarcinoma, sponsored by Tracon Pharmaceuticals.

NCT02396511 is a Phase 2 study of Choriocarcinoma that has completed, run by Tracon Pharmaceuticals. The registered enrollment target is 2 participants, below the 368-participant average among 5 other Choriocarcinoma trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02396511, a Phase 2 study of Choriocarcinoma, has completed, sponsored by Tracon Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
2 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine whether TRC105 in combination with Bevacizumab is effective in the treatment of two patients with metastatic and refractory choriocarcinoma.

Primary Outcome

Progression Free Survival of Two Patients With Metastatic and Refractory Choriocarcinoma determined according to RECIST 1.1 including measurement of serum β- hCG. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, a measurable increase in a non-target lesion, or the appearance of new lesions. A 5 mm absolute increase is also required to guard against over calling PD when the tot

Conditions Studied

Interventions

  • BIOLOGICAL Bevacizumab
  • BIOLOGICAL TRC105

Study Locations (1)

Massachusetts

  • Dana-Farber Cancer Insititue - Boston

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2015-01
Est. Completion 2017-12
Phase Phase 2
Tracon Pharmaceuticals

16 total trials

What the finished NCT02396511 record still lists

NCT02396511 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 368-participant average among 5 other Choriocarcinoma trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Choriocarcinoma appearing as the primary indexed condition, and to 2 interventions - of which Bevacizumab is the first listed.

NCT02396511 reports a single indexed study location in Massachusetts.

Frequently Asked Questions

What is clinical trial NCT02396511 about?

NCT02396511 is a clinical study titled "TRC105 Combined With Standard-dose Bevacizumab for Two Patients With Metastatic And Refractory Choriocarcinoma". The purpose of this study is to determine whether TRC105 in combination with Bevacizumab is effective in the treatment of two patients with metastatic and refractory choriocarcinoma.

What is the current status of trial NCT02396511?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 2 participants. The study started on 2015-01. Estimated completion is 2017-12.

What conditions does trial NCT02396511 study?

This clinical trial studies the following conditions: Choriocarcinoma.

What interventions are being tested in trial NCT02396511?

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

Who is sponsoring clinical trial NCT02396511?

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

Where is trial NCT02396511 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT02396511, the US trial registry maintained by the National Library of Medicine. NCT02396511 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.