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Completed Phase 1 Interventional

A Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors

ClinicalTrials.gov ID: NCT02432326

Public ClinicalTrials.gov record NCT02432326. 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 Sep 2, 2026, 12:10 PM 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 Ib Clinical Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors

Brief summary

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

This is an open label, multi-center, phase 1 study of BBI608 and BBI503 administered orally in combination to patients with advanced solid tumors. The primary goal is to determine the safety, tolerability, and recommended phase II dose (RP2D) of the combination regimen.

Study identification

NCT ID
NCT02432326
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Sumitomo Pharma America, Inc.
Industry
Enrollment
147 participants

Conditions and interventions

Interventions

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
Mar 31, 2015
Primary completion
Nov 30, 2019
Completion
Mar 31, 2020
Last update posted
Nov 7, 2023

2015 – 2020

United States locations

U.S. sites
11
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
University of Chicago Medicine Comprehensive Cancer Center Chicago Illinois 60637
Indiana University Simon Cancer Center Indianapolis Indiana 46202
Weill Cornell Medical College New York New York 10065
Texas Oncology - Austin Midtown Austin Texas 76104
Texas Oncology - Baylor Charles A. Sammons Cancer Center Dallas Texas 75246
Texas Oncology - Fort Worth 12th Ave Fort Worth Texas 76104
Texas Oncology, P.A. San Antonio Texas 78217
Texas Oncology, P.A. San Antonio Texas 78229
Texas Oncology - Tyler Tyler Texas 75702
Virginia Cancer Specialists, PC Fairfax Virginia 22031
Northwest Cancer Specialists, PC Vancouver Washington 98684

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 NCT02432326, 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 7, 2023 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02432326 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →