Spots Global Cancer Trial Database for A Study Evaluating the Safety, Tolerability, and Pharmacokinetics of GDC-0425 Administered With and Without Gemcitabine in Patients With Refractory Solid Tumors or Lymphoma
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Trial Identification
Brief Title: A Study Evaluating the Safety, Tolerability, and Pharmacokinetics of GDC-0425 Administered With and Without Gemcitabine in Patients With Refractory Solid Tumors or Lymphoma
Official Title: An Open-Label, Phase I, Dose Escalation Study Evaluating the Safety, Tolerability, and Pharmacokinetics of GDC-0425 Administered With and Without Gemcitabine in Patients With Refractory Solid Tumors or Lymphoma
Study ID: NCT01359696
Conditions
Study Description
Brief Summary: This is an open-label, multicenter, Phase I, dose-escalation study to assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of GDC-0425 administered with and without gemcitabine.
Detailed Description:
Keywords
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
Karmanos Cancer Institute.., Detroit, Michigan, United States
Sarah Cannon Cancer Center, Nashville, Tennessee, United States
Institut Gustave Roussy; Ser. de Med. Nucleaire; Cancerologie Endo, Villejuif, , France
Contact Details
Name: Chia Portera, M.D., Ph.D.
Affiliation: Genentech, Inc.
Role: STUDY_DIRECTOR
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