A Study of FOR46 in Patients With Relapsed or Refractory Multiple Myeloma (RRMM)

Completed · Phase 1

Conditions studied: Multiple Myeloma, Multiple Myeloma in Relapse, Multiple Myeloma With Failed Remission

In brief

This study will test the safety and efficacy of FOR46 given every 21 days to patients with relapsed or refractory multiple myeloma. The name of the study drug involved in this study is: FOR46 for Injection

Key facts

Study ID

NCT03650491

Run by

Fortis Therapeutics, Inc.

People needed

31

Starts

2019-04-03

Expected to finish

2022-01-31

Last updated by the study team

2022-07-27

Who can join

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

You may qualify if…

• Male or female ≥ 18 years of age
• Measurable MM that is relapsed or refractory to established therapies with known clinical benefit in RRMM or intolerant of those established MM therapies. Prior lines of therapy must include a proteasome inhibitor (PI), an immunomodulatory imide drug (IMiD) and a CD38-directed therapy in any order of combination.
• ECOG performance status of 0 or 1
• Adequate hematologic, renal and hepatic function
• Females of child-bearing potential must have a negative serum pregnancy test and use a medically acceptable form of contraception
• Male patients with with female partners of childbearing potential must agree to use 2 effective methods of contraception
• Patients must provide signed informed consent

You may not qualify if…

• Persistent clinically significant toxicities from previous anticancer therapy
• NCI CTCAE Grade ≥ 2 peripheral neuropathy from any etiology or has a genetic disorder that is associated with peripheral neuropathy even without current neuropathic manifestations
• Has received treatment with a stem cell transplant within 12 weeks before administration of patient's first dose of FOR46
• Has had radiation or systemic anticancer therapy within 14 days before first dose of FOR46
• Has received treatment with an investigational drug within 28 days before first dose of FOR46
• Has had a major surgical procedure within 28 days before administration of the patient's first FOR46 dose
• Is breastfeeding
• Clinically significant cardiovascular disease
• Uncontrolled, clinically significant pulmonary disease
• Uncontrolled intercurrent illness
• Has known positive status for HIV or either active/chronic hepatitis B/C
• Requires anticoagulation with warfarin or direct thrombin inhibitor; a washout of 7 days before the administration of a patient's first FOR46 dose is required for patients removed from these treatments
• Requires medications that are strong inhibitors or strong inducers of CYP3A4
• Has a history of episodic atrial fibrillation or flutter; patients with chronic atrial fibrillation are not excluded.
• Prior treatment with an ADC containing Monomethyl auristatin E (MMAE) or Monomethyl auristatin F (MMAF).

Where it is running

• UCSF Helen Diller Family Comprehensive Cancer Center — San Francisco, California, United States
• University of Colorado Cancer Center — Aurora, Colorado, United States
• Winship Cancer Institute, Emory University — Atlanta, Georgia, United States
• Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University — Baltimore, Maryland, United States
• Karmanos Cancer Institute — Detroit, Michigan, United States
• Washington University in St. Louis-Siteman Cancer Center — St Louis, Missouri, United States
• Icahn School of Medicine at Mt. Sinai — New York, New York, United States

Full record on ClinicalTrials.gov

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