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

NCT01204749 · ClinicalTrials.gov registry record · Phase 3

TRINOVA-1: A Study of AMG 386 or Placebo, in Combination With Weekly Paclitaxel Chemotherapy, as Treatment for Ovarian Cancer, Primary Peritoneal Cancer and Fallopian Tube Cancer

A Phase 3 study, sponsored by Amgen.

Completed
Registry status
Phase 3
Development phase
919
Enrollment target

NCT01204749: Completed Phase 3 study, sponsored by Amgen.

NCT01204749 is a Phase 3 study that has completed, run by Amgen. The registered enrollment target is 919 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (19% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01204749, a Phase 3 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 3
Development phase
919 participants
Enrollment target

Study Summary

The purpose of this study is to determine if treatment with paclitaxel plus AMG 386 is superior to paclitaxel plus placebo in women with recurrent partially platinum sensitive or resistant epithelial ovarian cancer, primary peritoneal cancer or fallopian tube cancer. AMG 386 is a man-made medication that is designed to stop the development of blood vessels in cancer tissues. Cancer tissues rely on the development of new blood vessels, a process called angiogenesis, to obtain a supply of oxygen and nutrients to grow.

Interventions

  • DRUG Paclitaxel
  • DRUG AMG 386
  • DRUG AMG 386 Placebo

Trial Details

FieldValue
Enrollment Target 919 participants
Start Date 2010-11
Est. Completion 2016-12
Phase Phase 3
Amgen

558 total trials

What the finished NCT01204749 record still lists

NCT01204749 is an interventional study that assigns participants to a tested intervention. The registered 919 participants enrollment target is mid-sized for trials with a published cap, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (19% higher).

The record links to 0 conditions, and to 3 interventions - of which Paclitaxel is the first listed.

NCT01204749 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01204749 about?

NCT01204749 is a clinical study titled "TRINOVA-1: A Study of AMG 386 or Placebo, in Combination With Weekly Paclitaxel Chemotherapy, as Treatment for Ovarian Cancer, Primary Peritoneal Cancer and Fallopian Tube Cancer". The purpose of this study is to determine if treatment with paclitaxel plus AMG 386 is superior to paclitaxel plus placebo in women with recurrent partially platinum sensitive or resistant epithelial ovarian cancer, primary peritoneal cancer or fallopian tube cancer. AMG 386 is a man-made medicatio...

What is the current status of trial NCT01204749?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 919 participants. The study started on 2010-11. Estimated completion is 2016-12.

What interventions are being tested in trial NCT01204749?

The interventions under investigation include: Paclitaxel (DRUG), AMG 386 (DRUG), AMG 386 Placebo (DRUG).

Who is sponsoring clinical trial NCT01204749?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01204749's enrollment target sits among peer trials

919 347th of 2000 higher than 1,654 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

  • NCT04589845 · 920 participants · Phase 2

    Tumor-agnostic Precision Immuno-oncology and Somatic Targeting Rational for You (TAPISTRY) Platform Study

  • NCT06109870 · 920 participants · NA

    Prevención en Sus Manos: Feasibility of a Novel Community-Based Strategy to Improve Access to Cervical Cancer Screening

  • NCT06957366 · 920 participants · NA

    Perioperative Anticoagulant Use for Surgery Evaluation -2 (PAUSE-2) Study Patients Receiving a Direct Oral Anticoagulant (DOACs-Dabigatran, Rivaroxaban, Apixaban or Edoxaban) and Needing Elective High-Bleed-Risk Surgery or an Invasive Procedure

  • NCT07174336 · 920 participants · Phase 3

    A Study of Tersolisib (LY4064809/STX-478) With Other Anti-Cancer Treatments in Participants With Advanced Breast Cancer With a Genetic Change (PIK3CA)

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 NCT01204749, the US trial registry maintained by the National Library of Medicine. NCT01204749 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.