Prostate Cancer Clinical Trial

Dose-Escalation and Safety Study of APC-100 for the Treatment of Prostate Cancer

Summary

This study is a phase 1/2a, open label, dose escalation and safety study of APC-100 (2,2,5,7,8-Pentamethyl-6-chromanol) in men with advanced prostate cancer.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients with histopathologically proven adenocarcinoma of the prostate
Patients must have progressive disease
Patients must have had prior treatment with bilateral orchiectomy or androgen deprivation therapy with an LHRH-blocker with evidence of treatment failure

Exclusion Criteria:

Patients treated with other secondary hormonal therapies
Patients with prior chemotherapy given for castrate-resistant prostate cancer
Patients with prior radiation therapy completed less than 4 weeks prior enrollment
Patients with prior investigational therapies within 4 weeks before treatment with APC-100
Evidence of active second malignancy

Study is for people with:

Prostate Cancer

Phase:

Phase 1

Estimated Enrollment:

60

Study ID:

NCT01436214

Recruitment Status:

Unknown status

Sponsor:

Adamis Pharmaceuticals Corporation

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 2 Locations for this study

See Locations Near You

Karmanos Cancer Institute
Detroit Michigan, 48201, United States
University of Wisconsin Carbone Cancer Center
Madison Wisconsin, 53705, United States

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 1

Estimated Enrollment:

60

Study ID:

NCT01436214

Recruitment Status:

Unknown status

Sponsor:


Adamis Pharmaceuticals Corporation

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider