A Phase 1-1b Study to Evaluate the Safety, Efficacy and Dosimetry of Study Drug A9-3408 in Subjects With Metastatic Melanoma

Recruiting now · Phase 1

Conditions studied: Melanoma Metastatic, Uveal Melanoma, Metastatic, Mucosal Melanoma

In brief

The goal of this trial is to see if this investigational drug is safe for adult patients with melanoma that has spread to other parts of the body or cannot be removed by surgery. It will also see if this investigational drug can shrink melanoma tumors in the body. The main questions this study aims to answer are: * What are the side effects of this investigational drug? * What is the highest dose of this investigational drug that can be given safely? Participants will: * Take the investigational drug once every 6 weeks, for up to 6 times in total * Visit a doctor's office on a regular basis for checkups and tests

Key facts

Study ID

NCT07076550

Run by

Alpha-9 Oncology USA Inc.

People needed

50

Starts

2025-11-19

Expected to finish

2028-01-01

Last updated by the study team

2026-03-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Able to provide written informed consent
• [68Ga]Ga-A9T-3202 uptake in at least one measurable lesion (per RECIST v1.1) on PET scan
• Histologically or cytologically confirmed unresectable or metastatic melanoma with disease progression on prior standard of care therapy
• Adequate ECOG performance status
• Adequate baseline organ function within 14 days of first dose of investigational product
• Recovered from side effects of prior anticancer therapy
• Women of childbearing potential (WOCBP) must have a negative pregnancy test and follow adequate birth control method(s) during the treatment period and for at least 6 months after last dose of [225Ac]Ac-A9-3408. Sexually active males with partners who are WOCBP must agree to adequate birth control method(s) during the treatment period and for at least 3 months after last dose of [225Ac]Ac-A9-3408

You may not qualify if…

• Previous treatment with radioactive nuclides except radioactive imaging tracers
• Treatment with another investigational product shortly prior to first dose of [225Ac]Ac-A9-3408 with exception of anti-PD-1/PD-L1 agents.
• Concurrent anticancer therapy
• Major surgery within 4 weeks of first dose of investigational product
• Second malignancy within 2 years
• Active, clinically serious infection
• Known infusion reactions to components of the investigational product
• Other clinically serious health conditions including cardiovascular and or severe infectious diseases
• Significant central nervous system metastatic disease
• Pregnant, breastfeeding or unwilling to practice adequate birth control method(s)
• Any condition per the opinion of the investigator that would impact the safety of the subject, protocol adherence or ability to provide informed consent

Where it is running

• Alfred Health — Melbourne, Victoria, Australia (enrolling)
• Austin Health — Melbourne, Victoria, Australia (enrolling)
• Fiona Stanley Hospital — Murdoch, Western Australia, Australia
• GenesisCare Murdoch — Murdoch, Western Australia, Australia

Full record on ClinicalTrials.gov

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