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Magic mushrooms can treat medication-resistant depression—but are they safe?

Magic mushrooms can treat medication-resistant depression—but are they safe?
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Akhila yerubandiJoshua caballeroCollege of pharmacyUniversity of georgiaNational institutes of healthNational institutesAcute adverse effectsTherapeutic doses

Is psilocybin safe for treating depression and anxiety?

A study in JAMA Network Open examined the acute adverse effects of therapeutic doses of psilocybin for treating depression and anxiety, focusing on its safety profile by assessing the occurrence of immediate side effects like headache, nausea, and elevated blood pressure among others.

Adverse effectsTherapeutic dosesSystematic reviewImage creditPreferred reporting itemsSystematic reviewsBlood pressureMental health

aTyr Pharma Announces Second Quarter 2023 Results and Provides Corporate Update

Phase 3 EFZO-FIT™ study of efzofitimod in pulmonary sarcoidosis currently enrolling in the U.S., Europe and Japan.

Sanjays shuklaAshlee dunstonCommittee for orphan medicinal productsEuropean respiratory societyPangu biopharmaEuropean commissionInternational congressPublic affairsAtyr pharma incEuropean medicines agencyTyr pharmaChief executive officerSubsequent periodOrphan medicinalNovel therapeutic candidateTherapeutic doses

United Therapeutics to Feature Clinical Data Across its Commercial and Development Portfolio at Upcoming Scientific Meetings

Results from the EXPEDITE study of Remodulin® induction prior to Orenitram® therapy to be presented at ATS Baseline patient data from the TETON studies of Tyvaso® Inhalation Solution in. | April 18, 2023

United statesHotel washingtonDistrict of columbiaFairfax hospitalAndrew nelsenJames gagermeierColleen mcevoySean francoisJorge malleaNader moazamiKarim el kershRobert montgomeryInformationfor remodulinSandeep sahaySteven nathanRaymond benza

ASLAN Pharmaceuticals Announces Positive Interim Data From the Multiple Ascending Dose Study of ASLAN004 in Atopic Dermatitis

- 74% average reduction in EASI from baseline at therapeutic doses after 8 weeks. 89% of patients achieved EASI-50 and 56% achieved EASI-90 - Data supportive of ASLAN004’s potential as a novel, first-in-class antibody targeting IL-13R with differentiated efficacy and safety profile in atopic dermatitis - Management to host conference call and webcast today, 1 March, at 8am ET / 9pm SGT SINGAPORE, March 01, 2021 (GLOBE NEWSWIRE) ASLAN Pharmaceuticals (Nasdaq:ASLN), a clinical-stage immunology focused biopharmaceutical company developing innovative treatments to transform the lives of patients, today announced positive interim unblinded data from the three dose cohorts of its ongoing randomised, double-blind placebo controlled multiple ascending dose study of ASLAN004 for the treatment of moderate to severe atopic dermatitis (AD). ASLAN004 was shown to be well tolerated across all doses and showed improvements compared to placebo in all efficacy endpoints, supporting its potenti

Atopic dermatitisTherapeutic dosesSafety profileThe companyசிகிச்சை அளவுகள்பாதுகாப்பு ப்ரொஃபைல்தி நிறுவனம்