Enlivex Announces Authorization from the Danish Regulatory Agency for the Company’s Randomized, Controlled Phase I/II Trial Evaluating Allocetra in Patients with Knee Osteoarthritis

https://www.globenewswire.com/news-release/2024/04/16/2863512/0/en/Enlivex-Announces-Authorization-from-the-Danish-Regulatory-Agency-for-the-Company-s-Randomized-Controlled-Phase-I-II-Trial-Evaluating-Allocetra-in-Patients-with-Knee-Osteoarthritis.html

Nes-Ziona, Israel, April 16, 2024 (GLOBE NEWSWIRE) — Enlivex Therapeutics Ltd. (Nasdaq:ENLV, the “Company”), a clinical-stage macrophage reprogramming immunotherapy company, today announced that the Danish Medicines Agency (DKMA) authorized the expansion into Denmark of the Company’s multi-country, randomized, controlled Phase I/II trial evaluating AllocetraTM in up to 160 patients with moderate to severe knee osteoarthritis. As previously announced, the Company received its first regulatory approval for this trial from the Israeli Ministry of Health (IMOH) in January.

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