177Lu-PSMA, Niraparib/AA Plus Prednisone for Prostate Cancer

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

WITHDRAWN

Clinical Phase

PHASE1/PHASE2

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-31

Study Completion Date

2028-10-31

Brief Summary

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The purpose of this research study is to test the safety and possible side effects of Lutetium-177 (177Lu)-Prostate-Specific Membrane Antigen (PSMA)-617 along with niraparib and abiraterone acetate plus prednisone when it is given to people diagnosed with metastatic castration-resistant prostate cancer (prostate cancer that has spread to other parts of the body and does not improve with hormonal therapies) at different dose levels. Once an optimal dose is selected, the researchers want to find out what how well these treatments work to improve survival and control the growth of the tumor.

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Detailed Description

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Conditions

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Metastatic Prostate Cancer Castration-resistant Prostate Cancer 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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177Lu-PSMA-617 in Combination with Niraparib/Abiraterone Acetate plus Prednisone

177Lu-PSMA-617 will be administered per standard of care at 7.4 gigabecquerel (GBq) (200 mCi) via intravenous (IV) infusion once every cycle (6 weeks) for 6 cycles. Niraparib/Abiraterone Acetate (Nira/AA) will be taken orally by the participant daily until disease progression or unacceptable toxicity. The starting dose level is 150 mg/1000 mg Nira/AA. Other dose levels include 200 mg/1000 mg, 100 mg/1000 mg, or 50 mg/500 mg Nira/AA once daily. Prednisone (5 mg) will be taken orally by the participant twice daily each day that Nira/AA is taken.

Group Type EXPERIMENTAL

177Lu-PSMA-617

Intervention Type DRUG

7.4 GBq (200 mCi) via IV infusion once every 6 weeks for 6 cycles

Niraparib abiraterone acetate

Intervention Type DRUG

Dual action drug tablet that is taken orally by the participant once per day in one of the following dose combinations depending on the cohort assignment and number of dose-limiting toxicities: 200 mg/1000 mg, 150 mg/1000 mg, 100 mg/1000 mg, 50 mg/500 mg

Prednisone

Intervention Type DRUG

5 mg orally twice per day

Interventions

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177Lu-PSMA-617

7.4 GBq (200 mCi) via IV infusion once every 6 weeks for 6 cycles

Intervention Type DRUG

Niraparib abiraterone acetate

Dual action drug tablet that is taken orally by the participant once per day in one of the following dose combinations depending on the cohort assignment and number of dose-limiting toxicities: 200 mg/1000 mg, 150 mg/1000 mg, 100 mg/1000 mg, 50 mg/500 mg

Intervention Type DRUG

Prednisone

5 mg orally twice per day

Intervention Type DRUG

Other Intervention Names

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Pluvicto Akeega Rayos Prednisone Intensol Deltasone

Eligibility Criteria

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Inclusion Criteria

* Signed informed consent must be obtained prior to participation in the study
* Adults ≥ 18 years of age
* Eastern Cooperative Oncology Group (ECOG) performance score of 0 to 2
* Life expectancy of greater than six months as determined by the treating physician
* Evidence of metastatic castration resistant prostate cancer with histological or cytology confirmed adenocarcinoma. This can be based on prior biopsy of prostate or metastatic disease.

1. Should have previous therapy with at least one androgen receptor pathway inhibitor in castration resistant or sensitive setting, and
2. Should have prior therapy with at least one line of therapy with taxane chemotherapy in castration resistant or sensitive setting
* Evidence of disease progression on current therapy which is based on either:

1. PSA progression: based on rising values at a minimum of 1-week intervals. The minimum starting value of PSA being 1 ng/mL
2. Radiologic progression: growth of known metastases or evidence of new metastases.
* Evidence of PSMA positive disease based on PSMA positron emission tomography (PET)/computed tomography (CT) scan utilizing radiotracers F-18 piflufolastat PSMA or Ga-68 PSMA-11. PSMA positive is defined as having at least one tumor lesion with radiotracer uptake greater than normal liver. Patients will be excluded if any lesions exceeding size criteria in short axis \[organs ≥ 1 cm, lymph nodes ≥ 2.5 cm, bones (soft tissue component) ≥ 1 cm\] have uptake less than or equal to uptake in normal liver.
* Patients must have evidence of metastatic disease with at least one of the following:

1. Metastatic disease in the bones visible on technetium-99m-MDP (methylene diphosphonate) bone scan ("bone scan") and/or
2. Pathologically enlarged lymph nodes of any distribution and/or
3. Visceral metastasis of any size or distribution.
* Adequate organ function:

1. Bone marrow reserve: absolute neutrophil count (ANC) ≥ 1500 cells/microliter (uL), platelets ≥ 100,000 cells/uL, hemoglobin ≥ 9 g/dL
2. Hepatic function: total bilirubin ≤ 2 × institutional upper limit of normal (ULN), for patients with known Gilbert syndrome ≤ 3 × institutional ULN is permitted. Alanine transaminase (ALT) or aspartate transaminase (AST) ≤ 3 × institutional ULN or ≤ 5 × institutional ULN if liver metastases
3. Renal function: estimated glomerular filtration rate (eGFR) ≥ 45 mL/min
* Able to swallow the study medication tablets whole.
* While on study medication and for 4 months following the last dose of study medication, participants must agree to use condom and an adequate contraception method for partner of childbearing potential. Participants must agree not to donate sperm while on study treatment and for a minimum of 4 months following the last dose of study medication.

Exclusion Criteria

* Pathological finding consistent with small cell or neuroendocrine carcinoma of the prostate
* Prior therapy with poly adenosine diphosphate (ADP)-ribose polymerase (PARP) inhibitor
* Prior therapy with 177Lu-PSMA 617 therapy. Exception: prior therapy with radium 223 is allowed if last dose was ≥ 6 months from study therapy. Note that other prior radiation therapy (such as external beam radiation therapy or brachytherapy) to prostate or other metastatic sites is allowed.
* History of adrenal dysfunction
* Active malignancies (i.e., progressing or requiring treatment change in the last 24 months) other than the disease being treated under study. The only allowed exceptions are:

1. Non-muscle invasive bladder cancer
2. Skin cancer (non-melanoma or melanoma) treated within the last 24 months that is considered completely cured
3. Malignancy that is considered cured with minimal risk of recurrence
* History or current diagnosis of myelodysplastic syndrome/acute myeloid leukemia (MDS/AML)
* Current evidence within 3 months of study consent of any of the following: severe/unstable angina, myocardial infarction, symptomatic congestive heart failure, clinically significant arterial or venous thromboembolic events (i.e., pulmonary embolism), or clinically significant ventricular arrhythmias.
* Presence of sustained uncontrolled hypertension (systolic blood pressure \>160 mm Hg or diastolic blood pressure \>100 mm Hg). Participants with a history of hypertension are allowed, provided that blood pressure is controlled to within these limits by an antihypertensive treatment.
* Known allergies, hypersensitivity, or intolerance to the excipients of Nira/AA tablets.
* Current evidence of any medical condition that would make prednisone use contraindicated.
* Received an investigational intervention (including investigational vaccines) or used an invasive investigational medical device within 30 days before the planned first dose of study medication
* Participants who have had the following ≤ 28 days prior to enrollment

1. A transfusion (platelets or red blood cells);
2. Hematopoietic growth factors;
3. Major surgery
* Participants with known history of human immunodeficiency virus with 1 or more of the following:

1. Not receiving highly active antiretroviral therapy or on antiretroviral therapy for less than 4 weeks
2. Receiving antiretroviral therapy that may interfere with the study medication
3. CD4 (type of white blood cell) count \<350 at screening.
4. An acquired immunodeficiency syndrome-defining opportunistic infection within 6 months of the start of screening.
5. Human immunodeficiency virus load \>400 copies/mL
* Known history of active or symptomatic viral hepatitis or chronic liver disease; encephalopathy, ascites or bleeding disorders secondary to hepatic dysfunction.
* Moderate or severe hepatic impairment (Class B and C per Child-Pugh classification system).

Minimum Eligible Age

18 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No