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Completed Phase 1Phase 2 Interventional Results available

Olaparib and Ramucirumab in Treating Patients With Metastatic or Locally Recurrent Gastric or Gastroesophageal Junction Cancer That Cannot Be Removed by Surgery

ClinicalTrials.gov ID: NCT03008278

Public ClinicalTrials.gov record NCT03008278. 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 Oct 21, 2026, 1:32 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

A Phase 1/2 Study of Olaparib in Combination With Ramucirumab in Metastatic Gastric and Gastroesophageal Junction Adenocarcinoma (10017760)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase I/II trial studies the side effects and best dose of olaparib when given together with ramucirumab and how well they work in treating patients with gastric or gastroesophageal junction cancer that has spread to other places in the body (metastatic), has come back (recurrent), or cannot be removed by surgery (unresectable). Olaparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as ramucirumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving olaparib and ramucirumab may work better in treating patients with gastric or gastroesophageal junction cancer compared to ramucirumab and paclitaxel (a chemotherapy drug) or ramucirumab alone.

Study identification

NCT ID
NCT03008278
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
51 participants

Conditions and interventions

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
Feb 6, 2018 (Actual)
Primary completion
Jun 30, 2023 (Actual)
Completion
Aug 13, 2025 (Actual)
Last update posted
Feb 3, 2026

2018 – 2025

United States locations

U.S. sites
32
U.S. states
10
U.S. cities
27
Facility City State ZIP Site status
City of Hope Corona Corona California 92882 —
City of Hope Comprehensive Cancer Center Duarte California 91010 —
City of Hope Antelope Valley Lancaster California 93534 —
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
UCSF Medical Center-Mount Zion San Francisco California 94115 —
City of Hope South Pasadena South Pasadena California 91030 —
City of Hope Upland Upland California 91786 —
Smilow Cancer Hospital-Derby Care Center Derby Connecticut 06418 —
Smilow Cancer Hospital Care Center-Fairfield Fairfield Connecticut 06824 —
Smilow Cancer Hospital Care Center - Guilford Guilford Connecticut 06437 —
Smilow Cancer Hospital Care Center at Saint Francis Hartford Connecticut 06105 —
Smilow Cancer Center/Yale-New Haven Hospital New Haven Connecticut 06510 —
Yale University New Haven Connecticut 06520 —
Yale-New Haven Hospital North Haven Medical Center North Haven Connecticut 06473 —
Smilow Cancer Hospital-Orange Care Center Orange Connecticut 06477 —
Smilow Cancer Hospital-Torrington Care Center Torrington Connecticut 06790 —
Smilow Cancer Hospital Care Center-Trumbull Trumbull Connecticut 06611 —
Smilow Cancer Hospital-Waterbury Care Center Waterbury Connecticut 06708 —
Smilow Cancer Hospital Care Center - Waterford Waterford Connecticut 06385 —
University of Florida Health Science Center - Gainesville Gainesville Florida 32610 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201 —
Weisberg Cancer Treatment Center Farmington Hills Michigan 48334 —
Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital New Brunswick New Jersey 08903 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
University of Pittsburgh Cancer Institute (UPCI) Pittsburgh Pennsylvania 15232 —
Vanderbilt Breast Center at One Hundred Oaks Nashville Tennessee 37204 —
Vanderbilt University/Ingram Cancer Center Nashville Tennessee 37232 —
M D Anderson Cancer Center Houston Texas 77030 —
University of Wisconsin Carbone Cancer Center - University Hospital Madison Wisconsin 53792 —

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 NCT03008278, 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 Feb 3, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03008278 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →