Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01669798 · ClinicalTrials.gov registry record · Phase 2

BIBF 1120 in Bevacizumab Resistant, Persistent, or Recurrent Epithelial Ovarian Cancer

A Phase 2 study, sponsored by AA Secord.

Completed
Registry status
Phase 2
Development phase
32
Enrollment target

NCT01669798: Completed Phase 2 study, sponsored by AA Secord.

NCT01669798 is a Phase 2 study that has completed, run by AA Secord. The registered enrollment target is 32 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (76% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01669798, a Phase 2 study, has completed, sponsored by AA Secord.

COMPLETED
Registry status
Phase 2
Development phase
32 participants
Enrollment target

Study Summary

The main purpose of this study is to see if BIBF 1120 can increase the number of women with bevacizumab resistant, persistent, or recurrent epithelial ovarian cancer who do not progress for at least six months.

Primary Outcome

Measure of Progression Free Survival (PFS) by the percentage of patients who survive progression-free for at least 6 months after initiating study therapy in patients with bevacizumab-resistant, persistent or recurrent epithelial ovarian, fallopian tube, or primary peritoneal carcinoma.

Interventions

  • DRUG BIBF 1120

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2013-02
Est. Completion 2018-02
Phase Phase 2
AA Secord

3 total trials

What the finished NCT01669798 record still lists

NCT01669798 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (76% lower).

The record links to 0 conditions, and to 1 intervention - of which BIBF 1120 is the first listed.

NCT01669798 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01669798 about?

NCT01669798 is a clinical study titled "BIBF 1120 in Bevacizumab Resistant, Persistent, or Recurrent Epithelial Ovarian Cancer". The main purpose of this study is to see if BIBF 1120 can increase the number of women with bevacizumab resistant, persistent, or recurrent epithelial ovarian cancer who do not progress for at least six months.

What is the current status of trial NCT01669798?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 32 participants. The study started on 2013-02. Estimated completion is 2018-02.

What interventions are being tested in trial NCT01669798?

The interventions under investigation include: BIBF 1120 (DRUG).

Who is sponsoring clinical trial NCT01669798?

This trial is sponsored by AA Secord, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01669798's enrollment target sits among peer trials

32 1563rd of 2000 higher than 423 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02445781 · 32 participants · Early Phase 1

    Differing Levels of Hypoglycemia

  • NCT02792270 · 32 participants · NA

    Caloric Restriction In Sarcoma Patients Treated With Pre-Operative RT

  • NCT03068910 · 32 participants · Early Phase 1

    Hyperandrogenemia and Altered Day-night LH Pulse Patterns

  • NCT03208868 · 32 participants · NA

    Leucine Enriched Essential Amino Acid Mixture to Reverse Muscle Loss in Cirrhosis

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01669798, the US trial registry maintained by the National Library of Medicine. NCT01669798 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.