Seelos Therapeutics Announces Updates to SLS-005 (trehalose) Programs for Europe and U.S.
Seelos Therapeutics, Inc. (SEEL)
Last seelos therapeutics, inc. earnings: 5/21 05:12 pm
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Source: GlobeNewswire
NEW YORK, Jan. 22, 2020 (GLOBE NEWSWIRE) -- Seelos Therapeutics, Inc. (Nasdaq: SEEL), a clinical-stage biopharmaceutical company focused on the development of therapies for central nervous system disorders and rare diseases, today announced an update regarding its development programs for SLS-005 (trehalose) in Europe and the U.S. Seelos has scheduled a meeting in March 2020 to meet with the European Medicines Agency (EMA) to seek scientific advice and protocol assistance for a European clinical study of SLS-005 in patients with Sanfillipo syndrome type A and B. The EMA provides support, including regulatory guidance and incentives, for the research and development of medicines for rare diseases in the European Union (EU). “We are truly excited to be working with the EMA to formulate the Sanfilippo study in the EU”, said Raj Mehra, Ph.D., Chairman and CEO of Seelos, “there are currently no approved therapies in the EU for this devastating neurological condition.” Additionally, S
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SEEL
Sec Filings
- 11/22/24 - Form NT
- 11/22/24 - Form 8-K
- 11/14/24 - Form SC
- SEEL's page on the SEC website