Safety Study to Assess AFM11 in Patients With Relapsed or Refractory Adult B-precursor ALL

Summary

The purpose of the study is to determine the maximum tolerated dose (MTD) in patients with acute lymphoblastic leukemia (ALL) and to determine the safety and tolerability of increasing doses and different infusion times of AFM11 infusion in patients with adult B-precursor ALL

Timeline

Start

2016-10

Primary completion

2018-09

Completion

2019-04

Outcome

Outcome not reported

Stopped (Business): “Strategic decision was made to terminate the AFM11 development”

Publications

• Topp M, Dlugosz-Danecka M, Skotnicki AB, Salogub G, Viardot A, Klein AK, Hess G, Michel CS, Grosicki S, Gural A, Schwarz SE, Pietzko K, Gartner U, Strassz A, Alland L, Mayer J. Safety of AFM11 in the treatment of patients with B-cell malignancies: findings from two phase 1 studies. Trials. 2023 Jan 3;24(1):4. doi: 10.1186/s13063-022-06982-7.

Drugs

Indications