A Phase I Study of [225Ac]-AZD2284 in Patients With Metastatic Castration-Resistant Prostate Cancer

AstraZeneca

Status and phase: Enrolling; Phase 1

Conditions: Metastatic Castration-Resistant Prostate Cancer

Treatments: Drug: AZD2287; Drug: AZD2275; Drug: AZD2284

Study type: Interventional

Funder types: Industry

Identifiers

NCT06879041

D7580C00001

Details and patient eligibility

About

The main purpose of the study is to assess the safety and tolerability of AZD2284, AZD2287, and AZD2275.

Full description

This is a first-in-human, Phase I, non-randomized, open-label clinical trial designed to evaluate AZD2284, AZD2287, and AZD2275.

This trial will consist of 2 Parts:

Part A (Imaging):

• Part A (Cold Antibody Exploration): aims to determine the optimal dosing regimen, with or without unconjugated antibody (AZD2275) pre-administration to improve the biodistribution of AZD2287.
• Part A Expansion: aims to explore the prevalence of PSMA and STEAP2 expression by imaging.

Part B (Therapeutic):

• Part B (Actinium-225 Dose Escalation): aims to assess the safety, tolerability, and efficacy of escalating doses of AZD2284 informed by the optimal dosing regimen identified in Part A.
• Part B Expansion Cohorts 1 and 2: aims to explore efficacy of AZD2284.

Enrollment: 134 estimated patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Main Inclusion Criteria:

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
• Histologically confirmed diagnosis of adenocarcinoma of the prostate or neuroendocrine differentiated prostate cancer.
• Must have had prior bilateral orchiectomy and/or ongoing androgen-deprivation therapy and a castrate level of serum/plasma testosterone (< 50 ng/dL or < 1.7 nmol/L).
• At least one metastatic lesion present on baseline Computed Tomography (CT), Magnetic Resonance Imaging (MRI), or bone scan obtained ≤ 28 days prior to the first dose of Investigational Medicinal Product (IMP). Participants may have non-measurable lesions including bone only metastases.
• Adequate organ function

Main Exclusion Criteria:

• Treatment with any radiopharmaceutical within 6 weeks of the first dose of Investigational Medicinal Product (IMP).
• Radiation therapy (RT) within 28 days prior to the first dose and all RT-related events have not recovered to Grade ≤ 1.
• Administration of any systemic cytotoxic or investigational therapy ≤ 28 days of the first dose of IMP or 5 half-lives, whichever is shorter.
• All prior treatment-related adverse events must have resolved to Grade ≤ 1.
• Concurrent severe and/or uncontrolled illness not related to cancer and/or social situation that would limit compliance with study requirements.
• Known or suspected allergies or contraindications to any of the investigational drugs or any component of the investigational drug formulation.
• Clinically relevant proteinuria

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Sequential Assignment

Masking: None (Open label)

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134 participants in 10 patient groups

Part A: Cohort A1: AZD2287 (Hot only)

Experimental group

Description:

Participants will receive 1 dose of AZD2287. If eligible for treatment, will receive low dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2287

Part A: Cohort A2: AZD2275 + AZD2287 (Cold +Hot)

Experimental group

Description:

Participants will receive low dose of AZD2275 followed by 1 dose of AZD2287. If eligible for treatment, will receive low dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part A: Cohort A3: AZD2275 + AZD2287 (Cold +Hot)

Experimental group

Description:

Participants will receive medium dose of AZD2275 followed by 1 dose of AZD2287. If eligible for treatment, will receive low dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part A Expansion: AZD2287 + AZD2275 (Cold + Hot)

Experimental group

Description:

Participants will receive dose of AZD2275 determined earlier in the study followed by 1 dose of AZD2287.

Treatment:

Drug: AZD2275

Drug: AZD2287

Part B (Actinium-225 Dose Escalation): low dose: AZD2284

Experimental group

Description:

Participants will receive AZD2287 (± AZD2275 as determined in Part A). If eligible for treatment, will receive low dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part B (Actinium-225 Dose Escalation): medium dose: AZD2284

Experimental group

Description:

Participants will receive AZD2287 (± AZD2275 as determined in Part A). If eligible for treatment, will receive medium dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part B (Actinium-225 Dose Escalation): high dose 1: AZD2284

Experimental group

Description:

Participants will receive AZD2287 (± AZD2275 as determined in Part A). If eligible for treatment, will receive high dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part B (Actinium-225 Dose Escalation): high dose 2: AZD2284

Experimental group

Description:

Participants will receive AZD2287 (± AZD2275 as determined in Part A). If eligible for treatment, will receive high dose of AZD2284.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part B: Cohort E1

Experimental group

Description:

Participants will receive dose of AZD2284 determined by the earlier results. Expansion cohort may be opened to further characterize the safety and efficacy of the dose level.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287

Part B: Cohort E2

Experimental group

Description:

Participants will receive dose of AZD2284 determined by the earlier results. Expansion cohort may be opened to further characterize the safety and efficacy of the dose level.

Treatment:

Drug: AZD2284

Drug: AZD2275

Drug: AZD2287