C3891001 - Integrin blockade in metastatic GU cancers (Renal Cell Carcinoma)

What is the Purpose of this Study?

If you choose to join this study you will:
- Receive study drugs called PF-06940434 and PF-06801591
-- PF-06940434 will be given via an IV every other week
-- PF-06801591 will be given subcutaneously (injected under your skin) once every 4 weeks
- Have blood and urine tests
- Send a tumor biopsy to the sponsor
- Have imaging tests (CT or MRI)
What is the Condition Being Studied?
Advanced or Metastatic Renal Cell Carcinoma

Who Can Participate in this Study?

Adults with advanced or metastatic renal cell carcinoma who:

- Are not able to have surgery to remove their cancer

- Have had one prior line of therapy that includes an immunotherapy against PD-(L)1 in combination with an anti-angiogenic treatment

For more information about who can join this study, contact the study team at julia.hurrelbrink@duke.edu.

Age Group
Adults
Participating Institutions

What is Involved?

We are doing this study to learn if a new study drug called PF-06940434 is safe and effective when given to people who have metastatic renal cell carcinoma in combination with another study drug, PF-06801591. Both of these drugs are types of antibodies that may target your tumor and increase your body’s immune response against the tumor tissue.

This study will also teach us how the study drugs are broken down by your body, and how your body's immune system is activated after you receive the study drugs.

Study Details

Full Title
C3891001 - A Phase 1 Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Escalating Doses of PF-06940434 in Patients with Advanced or Metastatic Solid Tumors
Principal Investigator

Protocol Number
IRB:
PRO00105876

NCT:
NCT04152018
ClinicalTrials.gov
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