Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06615752 · ClinicalTrials.gov registry record · Phase 1

Green Tea and Quercetin in Combination With Docetaxel Chemotherapy in Castration-resistant Prostate Cancer Patients

A Phase 1 study of Metastatic Castration-Resistant Prostate Cancer (mCRPC), sponsored by Charles Drew University of Medicine and Science.

Recruiting
Registry status
Phase 1
Development phase
99
Enrollment target
1
Study location

NCT06615752: Recruiting Phase 1 study of Metastatic Castration-Resistant Prostate Cancer (mCRPC), sponsored by Charles Drew University of Medicine and Science.

NCT06615752 is a Phase 1 study of Metastatic Castration-Resistant Prostate Cancer (mCRPC) that is actively recruiting participants, run by Charles Drew University of Medicine and Science. The registered enrollment target is 99 participants, below the 407-participant average among 15 other Metastatic Castration-Resistant Prostate Cancer (mCRPC) trials with a reported enrollment target (76% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06615752, a Phase 1 study of Metastatic Castration-Resistant Prostate Cancer (mCRPC), is actively recruiting participants, sponsored by Charles Drew University of Medicine and Science.

RECRUITING
Registry status
Phase 1
Development phase
99 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to find out if taking natural products green tea and quercetin along with docetaxel chemotherapy improves the therapy of advanced prostate cancer, i.e., metastatic castration-resistant prostate cancer (mCRPC). It will also learn about the safety of this combination. Researchers will compare green tea plus quercetin to a placebo (a look-alike substance that contains no drug) in combination with docetaxel to see if green tea and quercetin works to improve the therapeutic effect of docetaxel.

Primary Outcome

Blood PSA will be measured at baseline, 1st day of each cycle of docetaxel treatment (21 days per cycle, for 3 cycles), and at the end of the intervention.

Interventions

  • DRUG green tea and quercetin + docetaxel
  • DRUG Placebo + docetaxel

Study Locations (1)

California

  • Charles R. Drew University of Medicine and Science - Los Angeles

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2026-03
Est. Completion 2029-02
Phase Phase 1

What NCT06615752 shows while recruiting

NCT06615752 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 99 participants, a relatively small participant target, below the 407-participant average among 15 other Metastatic Castration-Resistant Prostate Cancer (mCRPC) trials with a reported enrollment target (76% lower).

The record links to 1 condition, with Metastatic Castration-Resistant Prostate Cancer (mCRPC) appearing as the primary indexed condition, and to 2 interventions - of which green tea and quercetin + docetaxel is the first listed.

NCT06615752 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT06615752 about?

NCT06615752 is a clinical study titled "Green Tea and Quercetin in Combination With Docetaxel Chemotherapy in Castration-resistant Prostate Cancer Patients". The goal of this clinical trial is to find out if taking natural products green tea and quercetin along with docetaxel chemotherapy improves the therapy of advanced prostate cancer, i.e., metastatic castration-resistant prostate cancer (mCRPC). It will also learn about the safety of this combination...

What is the current status of trial NCT06615752?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 99 participants. The study started on 2026-03. Estimated completion is 2029-02.

What conditions does trial NCT06615752 study?

This clinical trial studies the following conditions: Metastatic Castration-Resistant Prostate Cancer (mCRPC).

What interventions are being tested in trial NCT06615752?

The interventions under investigation include: green tea and quercetin + docetaxel (DRUG), Placebo + docetaxel (DRUG).

Who is sponsoring clinical trial NCT06615752?

This trial is sponsored by Charles Drew University of Medicine and Science, which has 30 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06615752 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Metastatic Castration-Resistant Prostate Cancer (mCRPC)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06615752's enrollment target sits among peer trials

99 13th of 15 higher than 3 of 15 other Metastatic Castration-Resistant Prostate Cancer (mCRPC) trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Metastatic Castration-Resistant Prostate Cancer (mCRPC) trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03965234 · 99 participants · Phase 1

    Pulmonary Suffusion in Controlling Minimal Residual Disease in Patients With Sarcoma or Colorectal Metastases

  • NCT04022616 · 99 participants

    Myeloid-Derived Suppressor Cell Function in Breast Cancer Patients

  • NCT04042844 · 99 participants · Phase 2

    A Single Dose of BRTX 100 for Patients With Chronic Lumbar Disc Disease (cLDD)

  • NCT04143724 · 99 participants · Phase 2

    Study of Safety & PK of Luspatercept (ACE-536) in Pediatric Participants With Beta (β)-Thalassemia

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT06615752, the US trial registry maintained by the National Library of Medicine. NCT06615752 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.