A Phase 2B Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Namodenoson in the Treatment of Non-Alcoholic Steatohepatitis (NASH)
Latest Information Update: 13 May 2024
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At a glance
- Drugs Namodenoson (Primary)
- Indications Non-alcoholic steatohepatitis
- Focus Adverse reactions; Therapeutic Use
- Sponsors Can-Fite BioPharma
- 09 May 2024 According to a Can-Fite Biopharma media release, company is enrolling patients for a Phase IIb clinical study in Europe and in Israel and the IND approval by FDA will allow for the recruitment of patients in the US.
- 09 May 2024 According to a Can-Fite Biopharma media release, company announced that U.S. Food and Drug Administration (FDA) has granted Investigational New Drug (IND) clearance for Namodenoson, for the treatment of patients with metabolic dysfunction-associated steatohepatitis (MASH), also known as non-alcoholic steatohepatitis (NASH), for the Company's ongoing Phase IIb clinical study.
- 15 Jun 2023 Planned End Date changed from 15 Apr 2023 to 15 Oct 2025.