Clinical Trial of Ac225-PSMA Radioligand Therapy of Metastatic Castration-resistant Prostate Cancer

NCT ID: NCT04225910

Last Updated: 2020-01-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

EARLY_PHASE1

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-01

Study Completion Date

2021-12-21

Brief Summary

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The death of prostate cancer patients is mainly due to metastatic castration-resistant prostate cancer. Though some new therapies has been tried to prolong the life-span of mCRPC patients, a dilemma was encountered for the drug-resistance. The PSMA RLT has been tested its efficacy and safety for the therapy of these patients. In our clinical trial, a new PSMA ligand will been used to be labeled with Ac225. This will be a prospective pilot clinical trial. 20 mCRPC patients who was incapable of 2rd ADT or chemotherapy will be recruited in this clinical tiral. The efficacy and safety of 225Ac-PSMA will be evaluated after the administration.

Detailed Description

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Conditions

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Metastatic Castration-resistant Prostate Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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mCRPC for PSMA RLT

225Ac-PSMA 100KBq/kg, iv. Totally 2 doses, every 8 weeks.

Group Type EXPERIMENTAL

225Ac-PSMA

Intervention Type DRUG

all the patients will receive 225Ac-PSMA RLT for 2 cycles. The dosage will be calculated according to 100KBq/kg body weight. The drug will be administered by vein injection.

Interventions

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225Ac-PSMA

all the patients will receive 225Ac-PSMA RLT for 2 cycles. The dosage will be calculated according to 100KBq/kg body weight. The drug will be administered by vein injection.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Pathologically confirmed prostatic adenocarcinoma.
* Clinically or imaging confirmed metastatic castration resistant prostate cancer.
* Conventional treatment failure or not available.
* PSMA avid of lesions confirmed by PSMA PET/CT.
* Hematopoietic function, kidney and liver function is normal.
* Can follow the study plan and can timely follow-up.
* Agree to sign the informed consent.

Exclusion Criteria

* Pathological types other than the prostatic adenocarcinoma of prostate cancer.
* Not PSMA avid of lesions confirmed by PSMA PET/CT.
* Concurrent with other uncontrolled malignant tumours or five years, except for carcinoma in situ.
* Concomitant diseases are not suitable for radioactive therapy.
* Other conditions (religion, psychology, etc.) affect the informed consent, research plan, or not compliant of follow-up schedule.
Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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Hui Wang, Professor

Role: CONTACT

86-021-25076980

Hongliang Fu

Role: CONTACT

86-021-25078591

References

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Other Identifiers

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XHEC-C-2019-042-2

Identifier Type: -

Identifier Source: org_study_id

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