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Clinical Trials/EUCTR2020-000209-10-DK
EUCTR2020-000209-10-DK
Active, not recruiting
Phase 1

A Phase II, Open-label Study to Assess the Efficacy, Safety, and Tolerability of AZD4635 in Combination with Durvalumab and in Combination with Cabazitaxel and Durvalumab in Patients Who Have Progressive Metastatic Castrate-Resistant Prostate Cancer (AARDVARC) - AARDVARC

AstraZeneca AB0 sites80 target enrollmentOctober 19, 2020

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Progressive Metastatic Castrate-Resistant Prostate Cancer
Sponsor
AstraZeneca AB
Enrollment
80
Status
Active, not recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 19, 2020
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1 Participant must be 18 years of age inclusive at the time of signing the informed consent.
  • 2 Histologically confirmed adenocarcinoma of the prostate.
  • 3 Known castrate\-resistant disease.
  • 4 Evidence of disease progression \=6 months.
  • 5 Body weight \>30 kg at screening.
  • 6 Willingness to adhere to the study treatment\-specific contraception requirements.
  • 7 Adequate bone marrow reserve and organ function.
  • 8 Adequate organ function for Arm A as demonstrated by all of the following laboratory values:
  • \- Alanine aminotransferase (ALT) \=2\.5 × upper limit of normal (ULN) if no demonstrable liver metastases or \=5 × ULN in the presence of liver metastases.
  • \- Aspartate aminotransferase (AST) \=2\.5 × ULN if no demonstrable liver metastases or \=5 × ULN in the presence of liver metastases

Exclusion Criteria

  • 1 Active brain metastases or leptomeningeal metastases.
  • 2 There must be no requirement for immunosuppressive doses of systemic corticosteroids for at least 2 weeks prior to study enrollment.
  • 3 History of pneumonitis, second malignancy that is progressing and/or received active treatment \=3 years before the first dose of study intervention, and hypersensitivity to polysorbate\-80 if allocated to cabazitaxel.
  • 4 As judged by the Investigator, any evidence of severe or uncontrolled systemic diseases.
  • 5 Creatinine clearance \<40 mL/min (calculated by Cockcroft\-Gault equation).
  • 6 Prior exposure to immune\-mediated therapy.
  • 7 History of allogeneic organ transplantation.\-
  • 8 Active or prior documented autoimmune or inflammatory disorders
  • 9 History of active primary immunodeficiency.
  • 10 Active infection including tuberculosis

Outcomes

Primary Outcomes

Not specified

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