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Folgendes wird aus ClinicalTrials.gov importiert:

A Phase 1/2 Study of CYT-0851 in B-Cell Malignancies and Advanced Solid Tumors

This clinical trial is an interventional, active-treatment, open-label, multi-center, Phase 1/2 study. The study objectives are to assess the safety, tolerability and pharmacokinetics (PK) of CYT-0851 in patients with relapsed/refractory B-cell malignancies and advanced solid tumors and to identify a recommended Phase 2 dose as a monotherapy and in combination with chemotherapy for evaluation in these patients.

Breast Cancer

Studiendesign
Studientyp:

Interventional

Geschätzte Einschreibung:

170 Teilnehmer

Aktueller Studienbeginn:

9. Oktober 2019

Zulassungskriterien
Alter für die Studie berechtigt:

18 - 999

Geschlechter für die Studie berechtigt:

both


Arms and Intervention
  • CYT-0851

  • CYT-0851 in combination with gemcitabine

  • CYT-0851 in combination with capecitabine

  • CYT-0851 in combination with rituximab and bendamustine

Trial Information at Site
Last Updated:
Studieninformationen
ClinicalTrial.gov ID:

Active, not recruiting

Estimated Enrollment:

170

Last Updated:

10/30/2023


Hauptermittler

Markus Renschler, MD


Studiensponsor

Cyteir Therapeutics, Inc.

Study Location (21)

Dana Farber Cancer Institute

Boston, Massachusetts, United States

Dana Farber Cancer Institute

Boston, Massachusetts, United States

John Theurer Cancer Center at HUMC

Hackensack, New Jersey, United States

Massachusetts General Hospital

Boston, Massachusetts, United States

Mayo Clinic

Jacksonville, Florida, United States

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