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NOT YET RECRUITING
NCT07316686
PHASE1

Phase I Study of Docetaxel and 177-Lutetium-PSMA-I&T in First-Line Treatment for Patients With Metastatic Castration-Resistant Prostate Adenocarcinoma

Sponsor: Instituto do Cancer do Estado de São Paulo

View on ClinicalTrials.gov

Summary

This is a Phase I, open-label, single-center study evaluating the safety, tolerability, and recommended Phase II dose of docetaxel when combined with a fixed dose of 177-Lutetium-PSMA-I\&T in chemotherapy-naïve patients with metastatic castration-resistant prostate cancer (mCRPC). Patients will receive standard androgen deprivation therapy, docetaxel at escalating doses (50 mg/m², 60 mg/m², 75 mg/m² every 3 weeks), and 177Lu-PSMA-I\&T at a fixed dose of 7.4 GBq every 6 weeks (up to 4 cycles). A 3+3 dose escalation design will be employed. Secondary endpoints include safety profile, treatment-limiting toxicities, treatment completion rate, and delayed toxicity. Exploratory endpoints include PSA response, radiographic progression-free survival (rPFS), and PERCIST-based response rate.

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2026-01

Completion Date

2026-12

Last Updated

2026-01-05

Healthy Volunteers

No

Interventions

DRUG

Docetaxel 50mg/m2

Intravenous, 50 mg/m², every 3 weeks, up to 10 cycles

DRUG

Docetaxel 60mg/m2

Intravenous, 60 mg/m², every 3 weeks, up to 10 cycles

DRUG

Docetaxel 75 mg/m²

Intravenous, 75 mg/m², every 3 weeks, up to 10 cycles

RADIATION

177Lu-PSMA-I&T

Intravenous administration at a fixed dose of 7.4 GBq every 6 weeks, up to 4 cycles.

Locations (1)

Instituto do Câncer do Estado de São Paulo - ICESP

São Paulo, São Paulo, Brazil