A Phase 1, First-in-human, Randomized, Double Blind, Placebo Controlled, Safety, Tolerability and Pharmacokinetic Study of ABY 039 in Healthy Subjects
Latest Information Update: 19 Jun 2020
At a glance
Most Recent Events
- 16 Jun 2020 Status changed from completed to discontinued.
- 15 Jun 2020 According to an Affibody media release, ABY-039 program is terminated due to tolerability observations that would limit the target product profile of subcutaneous high dose once monthly maintentance injections.The termination will become effective June 18, 2020.
- 15 Jun 2020 Status changed from recruiting to completed.