Description:
The therapy is administered at 8 ± 1week intervals, with the initial activity of 100 kBq/kg (±10%), then de-escalation to 87 kBq/kg (±10%), 75 kBq/kg (±10%) or 50 kBq/kg (±10%) in cases of good response (PSA decline >50%). The route of administration will be Intravenous (I.V.) infusion over approximately 1-3 minutes.
Sponsor:
Fusion Pharmaceuticals, Inc.Contacts:
Clinical Trials Fusion Pharmaceuticals Inc.clinicaltrials@fusionpharma.com
1 (888) 506-4125
Government Study Link:
NCT05219500 - Click here to see study onClinicalTrials.gov
Patient Education
Patient Education Not Yet Provided
Publications
Publications Not Yet Provided
Locations
17607 Gold Plaza, Omaha, Nebraska 68130, United States
Principal Investigator
Luke T. Nordquist, MD
Houston, Texas, United States
Principal Investigator
Ebrahim Delpassand, MD