Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New combo therapy targets Hard-to-Treat prostate cancer

NCT ID NCT07316686

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 26, 2026 · Updated 2 times

Summary

This early-stage trial tests a combination of two drugs—docetaxel (chemotherapy) and a radioactive compound called 177Lu-PSMA-I&T—in men with advanced prostate cancer that no longer responds to hormone therapy. The goal is to find the safest dose of docetaxel when used with the radioactive drug. Only 18 men will take part, and the study focuses on side effects and tolerability, not yet on how well the treatment works against the cancer.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
docetaxel and 177Lu-PSMA-I&T (a radioactive drug that targets prostate cancer cells)
What this could lead to
If this works, it could point toward a more effective first-line treatment for advanced prostate cancer that has stopped responding to hormone therapy.
What could go wrong
This is a very early Phase I trial with only 18 participants, so it is primarily testing safety and dosing. It is too small to prove whether the combination actually improves outcomes, and side effects from the chemotherapy and radiation could be significant.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

About 18 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2026

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Male participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Men aged 18 years or older. 2. Histological or cytological diagnosis of prostate adenocarcinoma. The presence of intraductal or cribriform carcinoma will be allowed. 3. Presence of metastatic disease on conventional imaging exams (bone scintigraphy and/or CT scan or MRI). 4. Patients with castration-resistant disease, defined as testosterone \<50 ng/mL in the context of prior orchiectomy or ongoing androgen deprivation therapy (ADT) with LHRH agonists or antagonists, plus at least one of the criteria below: 5. PSA ≥2.0 ng/mL with at least two consecutive PSA rises at intervals of at least 1 week. 6. Radiologic progression defined by the investigator. 7. Clinical progression defined by the investigator. 8. Performance status per the Eastern Cooperative Oncology Group (ECOG) equal to 0 or 1. 9. Willingness to continue ongoing ADT. 10. Adequate organ function as defined below: * Parameter Requirement * Neutrophils ≥ 1,500/µL * Hemoglobin ≥ 12 g/dL * Platelets ≥ 100,000/µL * Creatinine ≤ 1.5 x upper limit of normal * Potassium \> 3.5 mmol/L and \<5.0 mmol/L * Total Bilirubin ≤ ULN (unless Gilbert's disease) * AST (TGO) ≤ 2.5 x ULN * ALT (TGP) ≤ 2.5 x ULN 11. 68Ga-PSMA-PET/CT performed during the screening phase showing metastatic (extraprosthetic and extrapelvic) disease with radiotracer uptake and: 12. SUVmax ≥20 in at least one site; 13. SUVmax \>10 in all other measurable metastatic sites. 14. Lesions with uptake at least 1.5 times greater than hepatic background will be considered measurable. Exclusion Criteria: 1. Presence of any small-cell or neuroendocrine component of prostate carcinoma. 2. Prior receipt of chemotherapy or radiopharmaceuticals in the castration-resistant setting. 3. Presence of another active malignancy requiring treatment or a cancer diagnosis within the past 5 years. Carcinoma in situ of any site, squamous cell carcinoma of the skin, basal cell carcinoma of the skin, or papillary bladder tumors will be allowed if previously treated. 4. Severe urinary incontinence at the investigator's discretion. 5. 18F-FDG-PET/CT will be performed during screening and will be considered exclusionary if there is discordance with the 68Ga-PSMA-PET/CT. Discordance is defined as FDG-hypermetabolic lesions with absent or low PSMA uptake (SUVmax \<10) in more than 50% of measurable metastatic lesions. 6. Patients with brain metastases visible on 68Ga-PSMA-PET/CT.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Metastatic castration resistant prostate cancer are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Instituto do Câncer do Estado de São Paulo - ICESP

    RECRUITING

    São Paulo, 01246000, Brazil

More trials for these conditions

Other studies related to the condition(s) this trial covers.