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OncoMatch/Clinical Trials/NCT06139575

Phase 1/2 Clinical Study of Lutetium Lu 177 JH020002 Injection in Patients With Advanced Prostate Cancer

Is NCT06139575 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies Lutetium Lu 177 JH020002 for prostate cancer.

Phase 1/2RecruitingBivision Pharmaceuticals, Inc.NCT06139575Data as of Jun 2026Location: China

Treatment: Lutetium Lu 177 JH020002The study is being conducted to evaluate the safety, tolerability, pharmacokinetics, radiation dosimetry, and preliminary efficacy of Lutetium Lu 177 JH020002 Injection in adult patients with advanced prostate cancer.

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Extracted eligibility criteria

Treatments studied

Radioligand therapy

Lutetium Lu 177 JH020002

Cancer type

Prostate Cancer

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Male only

Prior therapy

Cannot have received: radioisotope therapy (Strontium-89, Samarium-153, Rhenium-186, Rhenium-188, Radium-223)

Exception: allowed if >6 months prior

Previous treatment with Strontium-89, Samarium-153, Rhenium-186, Rhenium-188, Radium-223 or hemi-body irradiation <6 months prior to date of first administration of investigational drug

Cannot have received: PSMA-targeted radioligand therapy

Previous PSMA-targeted radioligand therapy

Cannot have received: radiotherapy

Exception: allowed if >4 weeks prior

Previous radiotherapy for prostate cancer within 4 weeks prior to date of first administration of investigational drug

Cannot have received: systemic anti-cancer therapy (chemotherapy, immunotherapy, poly adenosine diphosphate-ribosyl polymerase inhibitors (PARPi), biological therapy)

Exception: allowed if >4 weeks prior

Any systemic anti-cancer therapy (e.g. chemotherapy, immunotherapy, poly adenosine diphosphate-ribosyl polymerase inhibitors (PARPi) or biological therapy within 4 weeks prior to date of first administration of investigational drug

Cannot have received: investigational therapy

Exception: allowed if >4 weeks prior

Must not take part in other investigational therapies within 4 weeks prior to date of first administration of investigational drug

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06139575 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior radioisotope therapy, PSMA-targeted radioligand therapy, radiotherapy disqualifies patients from enrollment.

Is this trial open to female patients?

No. This trial enrolls male patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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