Castration Resistant Prostate Cancer (CRPC)

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Review clinical trials related to Castration Resistant Prostate Cancer (CRPC). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Study of Oral MRT-2359 With Apalutamide in Prostate Cancer

This Phase 2, open-label, multicenter study is conducted in patients with castration-resistant prostate cancer. Patients in this study receive MRT-2359, an investigational oral medicine, in combination with apalutamide, an oral medicine used to treat prostate cancer. The main purpose of the study is to assess whether this treatment combination can lower prostate-specific antigen (PSA) The study will also evaluate the safety and tolerability of the treatment combination and assess additional measures of anti-tumor activity.

Participants needed: 25
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Monte Rosa Therapeutics, IncUpdated: Aug 4, 2026Locations: 14
Eligibility criteria

Age > 18 years [+10]

• Have received prior chemotherapy, definitive radiation, or biological cancer t... [+7]

Status: Not yet recruiting

Safety, Tolerability, and Efficacy of CP-PCA07 in Combination With Enzalutamide in Patients With Castration-Resistant Prostate Cancer

The purpose of this clinical study is to evaluate the safety, tolerability, and efficacy of CP-PCA07 in combination with enzalutamide in patients with castration-resistant prostate cancer (CRPC). This is an open-label, dose-escalation, multicenter Phase 1 study. The primary objective is to assess the maximum tolerated dose (MTD) and dose-limiting toxicities (DLTs) to determine the recommended Phase 2 dose (RP2D) of the combination therapy. The secondary objective is to assess changes in Prostate-Specific Antigen (PSA) levels and pharmacokinetic characteristics. Exploratory objectives include assessment of tumor response, disease control, progression-free survival, and biomarker analyses, including AR-V7 status, according to RECIST version 1.1 and other applicable criteria.

Participants needed: 18
Trial details
Phase: Phase 1Age: 19+Biological sex: MaleType: InterventionalSponsor: Hyundai Bioscience Co., Ltd.Updated: Jul 6, 2026Locations: 1
Eligibility criteria

1. Male patients aged ≥19 years at the time of providing written informed consen... [+7]

1. Patients who have received chemotherapy, chemoradiotherapy, biologic therapy,... [+17]

Status: Recruiting

A Study to Investigate the Safety, Pharmacokinetics, and Preliminary Efficacy of IDE574 Therapy in Adult Participants With Advanced Solid Tumors

IDE574 is a synthetically manufactured small molecule inhibitor that co-targets the lysine acetyltransferase enzymes KAT6 and KAT7. The purpose of this study is to evaluate the safety, preliminary efficacy, pharmacokinetics (PK), and pharmacodynamics (PD) of IDE574 as monotherapy in participants with locally advanced or metastatic solid tumors and as combination therapy with fulvestrant in participants with advanced or metastatic ER+, HER2- breast cancer.

Participants needed: 160
Trial details
Phase: Phase 1Age: 18-99Biological sex: AllType: InterventionalSponsor: IDEAYA BiosciencesUpdated: Jun 16, 2026Locations: 11
Eligibility criteria

Part 1A - Participants with advanced or metastatic ER+, HER2- breast cancer, NSC... [+8]

Known symptomatic brain metastases or leptomeningeal metastasis [+8]

Status: Recruiting

177Lu-BetaBart in Patients With Relapsed/Refractory, Locally Advanced Inoperable, or Metastatic Solid Tumors

A Phase 1/2a Dose Escalation and Expansion Study of the Safety, Tolerability, and Preliminary Clinical Activity of 177LuBetaBart, a 177Lu-Labeled Anti-B7-H3 Monoclonal Antibody, in Patients with Relapsed/Refractory, Locally Advanced Inoperable, or Metastatic Solid Tumors

Participants needed: 61
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Radiopharm Theranostics, LtdUpdated: Mar 27, 2026Locations: 4
Eligibility criteria

Willing and able to provide informed consent prior to start of any study procedu... [+2]

Participants must have documented disease progression during or after their most... [+44]