A Dose Escalation Study Evaluating the Safety and Tolerability of GDC-0032 in Participants With Locally Advanced or Metastatic Solid Tumors or Non-Hodgkin's Lymphoma (NHL) and in Combination With Endocrine Therapy in Locally Advanced or Metastatic Horm…

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

AN OPEN-LABEL, PHASE I/II, DOSE-ESCALATION STUDY EVALUATING THE SAFETY AND TOLERABILITY OF GDC-0032 IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC SOLID TUMORS AND IN COMBINATION WITH ENDOCRINE THERAPY IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC HORMONE RECEPTOR-POSITIVE BREAST CANCER

Intervention/treatment:
TASELISIB (GDC-0032)/ FLUDEOXYGLUCOSE 18F/ TECHNETIUM 99M TC PERTECHNETATE
Medical condition:
BREAST CANCER
Protocol code:
PMT4979G (GO00886)
Control number:
166813
Status:
Closed
Approved:
August 15, 2013
Date Completed:
Trial phase:
Phase 1
For more information:
ClinicalTrials.gov - NCT01296555
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Medical Communications
Organization
Hoffmann-La Roche
Phone:
800 821-8590
Sponsor
GENENTECH INC

Locations

Ontario

University Health Network; Princess Margaret Hospital; Medical Oncology Dept
Toronto, Ontario, M5G 2M9

Results

See the results from the trial NCT01296555. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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