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Completed Phase 1 Interventional Results available

Study of Niraparib, TSR-022, Bevacizumab, and Platinum-Based Doublet Chemotherapy in Combination With TSR-042

ClinicalTrials.gov ID: NCT03307785

Public ClinicalTrials.gov record NCT03307785. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 8:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 1b Dose-Finding Study of Niraparib, TSR-022, Bevacizumab, and Platinum-Based Doublet Chemotherapy in Combination With TSR-042 in Patients With Advanced or Metastatic Cancer

Study identification

NCT ID
NCT03307785
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Tesaro, Inc.
Industry
Enrollment
60 participants

Conditions and interventions

Interventions

  • Bevacizumab Drug
  • Carboplatin-Nab-Paclitaxel Drug
  • Carboplatin-Paclitaxel Drug
  • Carboplatin-Pemetrexed Drug
  • Niraparib Drug
  • TSR-022 Drug
  • TSR-042 Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 11, 2017
Primary completion
Feb 25, 2020
Completion
Dec 10, 2024
Last update posted
Nov 24, 2025

2017 – 2024

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
GSK Investigational Site Scottsdale Arizona 85258
GSK Investigational Site Encinitas California 92024
GSK Investigational Site San Marcos California 92069
GSK Investigational Site Sarasota Florida 34232
GSK Investigational Site Canton Ohio 44718
GSK Investigational Site Cleveland Ohio 44106
GSK Investigational Site Nashville Tennessee 37203
GSK Investigational Site Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03307785, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 24, 2025 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03307785 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →