Overview

Targeted Alpha Particle Radiotherapy for Metastatic Uveal Melanoma

Status:
Recruiting
Trial end date:
2029-02-25
Target enrollment:
0
Participant gender:
All
Summary
The primary aim of the study is to establish the maximum-tolerated dose (MTD) of 225Ac-MTI-201 in participants with metastatic uveal melanoma. The secondary aims are to describe the pharmacokinetics of 225Ac-MTI-201 and the toxic effects of 225Ac-MTI-201 in participants with metastatic uveal melanoma.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Modulation Therapeutics, Inc.
Collaborator:
H. Lee Moffitt Cancer Center and Research Institute
Criteria
Inclusion Criteria:

- Histologically confirmed metastatic uveal melanoma.

- Progression after at least one prior line of therapy for metastatic uveal melanoma.
Liver directed therapy (e.g., hepatic arterial embolization, isolated hepatic
perfusion) will count as one line of therapy. Should any additional treatment(s)
receive regulatory approval for metastatic uveal melanoma during the conduct of this
trial, participants (if eligible for the newly approved treatment) would need to
demonstrate disease progression on the additional treatment(s) before being eligible
to participate in the current study. There is no limit to the number of previous
treatments for metastatic disease.

- Participants must have measurable disease per RECIST 1.1.

- Adults, age 18 or over, with no upper age limit.

- ECOG performance status of 0-1 (Karnofsky ≥ 70 percent).

- Acceptable organ and marrow function as defined below:

- Leucocytes ≥ 3,000/μL

- Absolute neutrophil count ≥ 1,500/μL

- Platelets ≥ 100,000/μL

- Aspartate aminotransferase AST/ Alanine aminotransferase ALT ≤ 2.5x institutional
upper limit of normal (ULN)

- Bilirubin ≤ 1.5x institutional upper limit of normal (ULN)

- Creatinine clearance ≥ 60mL/min/1.73m^2 (measured by Cockcroft-Gault equation
using actual body weight in kilograms, and then adjusted for body surface area)

- Male participants who are sexually active, and female participants of childbearing
potential must agree to use 2 forms of FDA approved contraceptive methods during
treatment with 225Ac-MTI-201 and up to 3 months following treatment.

- Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

- Prior alpha-particle therapy.

- Has known symptomatic central nervous system (CNS) metastases and/or carcinomatous
meningitis. Participants with previously treated brain metastases may participate
provided they are stable without evidence of progression by imaging for at least four
weeks after definitive intervention and using no more than the equivalent of
dexamethasone 2 mg/d for the management of vasogenic edema, if necessary. This
exception does not include carcinomatous meningitis, which is excluded regardless of
clinical stability.

- Participants with an active malignancy requiring anticancer treatment at the time of
study entry that, in the judgment of the investigator could impact the results of
treatment of metastatic uveal melanoma.

- Pregnant or nursing women. Women of childbearing potential (defined as having had a
menstrual cycle within the past 12 months, and not having had a surgical procedure for
sterilization) must have a negative pregnancy test (urine or serum) within 7 days of
treatment with 225Ac-MTI-201.

- Participants with uncontrolled inter-current illness including, but not limited to,
ongoing or active bacterial infection, active hepatitis B/C infection requiring
antiviral therapy, symptomatic congestive heart failure, unstable angina pectoris,
cardiac arrhythmia, or psychiatric illness/social situations that would limit
compliance with study requirements.

- Immunocompromised participants may be at increased risk of toxicity. Therefore,
HIV-positive participants, participants with acquired or congenital immunodeficiency
conditions, those on chronic systemic corticosteroids requiring >10 mg of prednisone
or equivalent per day will be excluded from participation. (Participants with
autoimmune disease who do not require corticosteroids or are maintained on ≤10 mg of
prednisone or equivalent per day ARE eligible for participation; for participants with
CNS metastases on steroids, exclusion criterion bullet point #2 above will apply).

- Prior external beam radiation therapy to more than 25 percent of the bone marrow.