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FOR46 for Multiple Myeloma
Phase 1
Waitlist Available
Research Sponsored by Fortis Therapeutics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
A Study of FOR46 in Patients With Relapsed or Refractory Multiple Myeloma (RRMM)
Eligible Conditions
- Multiple Myeloma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Disease response
Incidence of adverse events
Occurrence of dose-limiting toxicities
Secondary outcome measures
Antidrug Antibodies
Characterize FOR46 elimination
Plasma
+4 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Experimental: FOR46 (Dose Expansion)Experimental Treatment1 Intervention
Eligible patients will receive FOR46 administered as an IV infusion every 21 days. Patients will receive the maximum tolerated dose during the Dose Expansion period of the study.
Group II: Experimental: FOR46 (Dose Escalation)Experimental Treatment1 Intervention
Eligible patients will receive FOR46 administered as an IV infusion every 21 days. Patients will be enrolled into escalating dose levels during the Dose Escalation period of the study.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
FOR46
2019
Completed Phase 1
~90
Find a Location
Who is running the clinical trial?
Fortis Therapeutics, Inc.Lead Sponsor
3 Previous Clinical Trials
116 Total Patients Enrolled
Andrew Dorr, MDStudy DirectorFortis Therapeutics, Inc.
1 Previous Clinical Trials
56 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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