Polaprezinc Treatment for Enzalutamide- or Abiraterone-resistant CRPC (PEACe)

Jiangnan University

Status and phase: Completed; Phase 2; Phase 1

Conditions: Castration-resistant Prostate Cancer

Treatments: Drug: Polaprezinc group; Drug: Control group

Study type: Interventional

Funder types: Other

Identifiers

NCT05549778

JiangnanU RWang-2

Details and patient eligibility

About

The purpose of this study is to evaluate clinical safety and efficacy of a gastric ulcer drug, polaprezinc (POL), with the AR-inhibitor abiraterone in Chinese patients with castration-resistant prostate cancer (CRPC).

Full description

Prostate cancer (PCa) is a major disease that affects 14.1% male population worldwide with a 6.8% mortality rate in 2020 (https://gco.iarc.fr/). In China, the PCa incidence rate is lower than in Europe and the US but increases rapidly. Androgen deprivation therapy (ADT) has been the most used treatment for men with advanced prostate cancer for decades. Despite the initial favorable response, nearly all patients progress to castration-resistant prostate cancer (CRPC) and subsequently succumb to the disease within 1-3 years.

Zinc-L-carnosine (ZnC), also called polaprezinc (otherwise known as PepZin GI™), is a chelated compound that contains L-carnosine and zinc. Some reports indicated that POL is effective in restoring the gastric lining, healing other parts of the gastrointestinal (GI) tract, improving taste disorders, improving GI disorders, and enhancing skin and liver. The primary mechanisms of POL action are identified as anti-inflammatory and antioxidant pathways. We have identified PRDX5 as a therapeutic target and repurposed polaprezinc (POL) as its inhibitor for the treatment of CRPC.

CRPC patients will be enrolled with their fully informed consent. Patients will be on abiraterone/prednisone, abiraterone/prednisone plus polaprezinc granules, or with other treatments according to patients' wishes in consultation with physicians. Polaprezinc will be 75 mg b.i.d., for 6 months. A standard regimen will be used for other treatments. PSA will be measured every month. ECT will be taken before and after treatment.

Enrollment: 12 patients

Sex: Male

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Male patients were older than 18 years of age.
2. Patients with measurable disease were required to have documented disease progression by Response Evaluation Criteria in Solid Tumors (RECIST) (28) with at least one bone metastatic lesion. Patients with non-measurable disease were required to have at least two consecutive increases (relative to a reference value measured at least a week apart) in serum PSA.
3. Patients had been taking abiraterone or enzalutamide for at least three consecutive months and showed a persistent rise in PSA.
4. Life expectancy >6 months

Exclusion criteria

1. Patients had taken polaprezinc previously.
2. Patients had cancer therapy (other than ADT) within 4 weeks before enrolment.
3. Patients had malignancies other than prostate cancer.
4. Patients had uncontrolled severe illness or medical conditions.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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12 participants in 2 patient groups

Polaprezinc group

Experimental group

Description:

Patients will be on abiraterone plus polaprezinc (75 mg b.i.d. for 6 months)

Treatment:

Drug: Polaprezinc group

Control group

Active Comparator group

Description:

Patients will be on abiraterone, radiotherapy or chemotherapy for 6 months

Treatment:

Drug: Control group