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Trial Phases

Phase 17
Phase 21

Trial Status

Completed7
Other1

Role Distribution

Other Roles8

Activity Timeline

Clinical Trials (8)

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1 collaborators·0 connections
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Current Investigator
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CO
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Clinical Trials (8)

Showing 8 of 8 trials

NCT01287091Phase 1StudyDirector

A 3-Part Study to Determine the Relative Bioavailability of Capsule and Tablet Formulations of GDC-0980, the Effect of Food, and the Effect of Rabeprazole on the Pharmacokinetics of the Tablet

Healthy Volunteer
Completed
NCT00999128Phase 1StudyDirector

A Study to Determine the Relative Bioavailability of Capsule and Tablet Formulations of GDC-0941 and the Effect of Food and Proton Pump Inhibition on GDC-0941 Tablet Pharmacokinetics in Healthy Volunteers

Healthy Volunteers
Completed
NCT00509769Phase 2StudyDirector

A Study of Trastuzumab Emtansine (Trastuzumab-MCC-DM1) Administered Intravenously to Patients With Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Metastatic Breast Cancer

Metastatic Breast Cancer
Completed
NCT00753480Phase 1StudyDirector

A Study of D4064A Administered to Patients With Recurrent or Persistent Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancer

Fallopian Tube CancerOvarian CancerPeritoneal Cancer
Suspended
NCT00932373Phase 1StudyDirector

A Study of Trastuzumab-MCC-DM1 Administered Intravenously to Patients With HER2-Positive Metastatic Breast Cancer Who Have Previously Received a Trastuzumab-Containing Regimen

Metastatic Breast Cancer
Completed
NCT01240226Phase 1StudyDirector

A Study to Determine the Relative Bioavailability of a Tablet Formulation of GDC-0941 and the Effect of Ketoconazole on the Pharmacokinetics of the GDC-0941 Tablet

Healthy Volunteer
Completed
NCT01356173Phase 1StudyDirector

Evaluating the Safety and Tolerability of GDC-0349 in Patients With Locally Advanced or Metastatic Solid Tumors or Non Hodgkin's Lymphoma

Non-Hodgkin's Lymphoma, Solid Tumor
Completed
NCT01474668Phase 1StudyDirector

Study to Investigate the Absorption, Metabolism, and Excretion of [14C]-GDC-0941 Following Single Oral Dose Administration in Healthy Male Subjects

Healthy Volunteer
Completed

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