A Study Evaluating the Safety and Pharmacokinetics of Escalating Doses of Forimtamig in Participants With Relapsed or Refractory Multiple Myeloma (r/r MM)

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

225

Participants

Timeline

Start Date

November 11, 2020

Primary Completion Date

February 20, 2026

Study Completion Date

February 20, 2026

Conditions
Multiple Myeloma
Interventions
DRUG

Forimtamig

Forimtamig will be administered via IV/SC administration. The RP2Ds determined during Part I: Dose Escalation will be administered during Part II: Dose Expansion. Forimtamig will be administered as per the dosing schedule defined in Part I.

Trial Locations (20)

1010

New Zealand Clinical Research - Auckland, Auckland

2100

Rigshospitalet, København Ø

3000

Peter MacCallum Cancer Center, Melbourne

5000

Odense Universitetshospital, Odense C

9000

UZ Gent, Ghent

20089

Instituto Clinico Humanitas, Rozzano

20133

Fond. IRCCS Istituto Nazionale Tumori, Milan

31008

Clinica Universitaria de Navarra, Pamplona

33604

Hopital De Haut Leveque, Pessac

37007

Hospital Clinico Universitario de Salamanca, Salamanca

39008

Hospital Universitario Marques de Valdecilla, Santander

40138

Policlinico S.Orsola-Malpighi, Bologna

44093

CHU NANTES - Hôtel Dieu, Nantes

59037

CHRU Lille - Hôpital Claude Huriez, Lille

80131

IRCCS Istituto Nazionale dei Tumori di Napoli - Pascale Ematologia Oncologica, Napoli

03080

Seoul National University Hospital, Seoul

06351

Samsung Medical Center, Seoul

06591

Seoul St Mary's Hospital, Seoul

LS9 7TF

St James University Hospital, Leeds

W1T 7HA

University College London Hospitals NHS Foundation Trust, London

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY