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Aquestive Therapeutics to Present Crossover Study Data for Libervant™ (diazepam) Buccal Film at

WARREN, N.J., April 12, 2024 (GLOBE NEWSWIRE) Aquestive Therapeutics, Inc. (NASDAQ: AQST) (the “Company” or “Aquestive”), a pharmaceutical company advancing medicines to bring meaningful improvement to patients lives through

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Tiziana Life Sciences Ltd : Tiziana Life Sciences Announces Platform Presentation of New Quantitative PET Imaging Data on Foralumab at the Annual Meeting of the American Academy of Neurology

Tiziana Life Sciences Ltd : Tiziana Life Sciences Announces Platform Presentation of New Quantitative PET Imaging Data on Foralumab at the Annual Meeting of the American Academy of Neurology
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United statesTarun singhalIrina kofflerPaul spencerDennis riedlTiziana life sciences ltdHarvard medical schoolLifesci advisorsMeeting of the american academy neurologyTiziana life sciencesProgram numberBusiness developmentNasal foralumab dampens microglial activationStabilizes clinical progressionNon active secondary progressiveClinical decision

Tiziana Life Sciences Announces Platform Presentation of New Quantitative PET Imaging Data on Foralumab at the Annual Meeting of the American Academy of Neurology - Tiziana Life Sciences (NASDAQ:TLSA)

NEW YORK, April 11, 2024 (GLOBE NEWSWIRE) Tiziana Life Sciences Ltd. (NASDAQ:TLSA) ("Tiziana" or the "Company"), a biotechnology company developing breakthrough neuro-immunomodulation therapies, today announced an

United statesIrina kofflerPaul spencerMeeting of the american academy neurologyLifesci advisorsTiziana life sciences ltdBusiness developmentTiziana life sciencesLife sciencesNasal foralumab dampens microglial activationStabilizes clinical progressionNon active secondary progressiveClinical decisionAnnual meetingAmerican academySci advisors

American Academy of Neurology (AAN)

American Academy of Neurology (AAN)News, press releases, and expert sources for journalists in science, medicine & business

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Minoryx gains FDA approval to initiate a Phase 3 clinical trial in patients with cerebral adrenoleukodystrophy

Minoryx gains FDA approval to initiate a Phase 3 clinical trial in patients with cerebral adrenoleukodystrophy  US trial with leriglitazone to commence in mid-2023 providing an FDA-approved route to US market whilst EMA evaluates European Marketing Authorization Application (MAA) Mataró, Barcelona,.

Comunidad autonoma de catalunaUnited statesMarc martinellAli fatemiEric mallackDrug administrationMeeting of the american academy neurologyKennedy krieger institute in baltimoreEuropean marketing authorization applicationX linked adrenoleukodystrophyHematopoietic stem cell transplantSouth americaKennedy krieger instituteGlobal principal investigatorLabel phaseChildhood cerebral