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25% of Patients Achieve Endoscopic Remission in Phase 2a EMERALD-1 Trial for MORF-057

Data from the phase 2a trial showed 25.7% of patients with UC demonstrated endoscopic improvement and 45.7% achieved clinical response after week 12.

United statesPbruce sandsPraveen tipirneniHenryd janowitzAlimentiv bruce sandsMount sinai health systemUnited european gastroenterology weekMount sinai healthRobarts histopathology indexMayo composite scorePresent positiveSevere ulcerative colitisMorphic reports positive topline resultsOrally administeredPrimary endpointOpen label study

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A look at the arguments for and against the use of medicinal cannabis

United kingdomTamil naduOdohertyj oconnorRay oconnorJournal of pain researchDravet syndrome study groupHealth research boardGarda press officeNational institute of healthA world health organisationRoyal college of psychiatristsCannabis sativaDrugs actRoyal collegeWorld health organisationCochrane systematic review

Study finds high doses of oral CBD can exacerbate THC s effects by inhibiting THC metabolism

Researchers compare the pharmacokinetics and pharmacodynamics of oral Δ9-tetrahydrocannabinol-dominant and cannabidiol-dominant cannabis extracts that contained the same Δ9-THC dose (20 mg).

Johns hopkins universityOrally administeredTetrahydrocannabinol pharmacokineticsHealthy adultsRandomized clinicalImage creditIndustry focusClinical trialCytochrome p450

Arvinas Reports Third Quarter 2022 Financial Results and

– On track to initiate enrollment of two Phase 3 trials with ARV-471 in patients with first- and second-line metastatic breast cancer – – Enrolling.

San antonioUnited statesJohn houstonJeff boyleJohn youngKirsten owensCompany board of directorsRegulatory affairsArvinas incExchange commissionDevelopment expensesPfizer incRockefeller universityPhoremost ltdSociety for neuroscienceSan antonio breast cancer symposium

Matinas BioPharma Provides Business Update and 2022 Strategic Outlook

25.01.2022 - – End of Phase 2 Meeting with FDA Provides Pathway to NDA Submission for MAT2203 Following Confirmatory Data to be Generated in an Additional Cohort; Cohort 5 in Ongoing EnACT Trial – – Cohort 4 of EnACT (all oral induction regimen) Underway With . Seite 1

Jeromed jabbourMatinas biopharma holdings incDrug administrationFund planned operationsVivo studyOrally administeredDemonstrated reduced viral titersEffects similarSubcutaneous administered remdesivirAdditional preclinicalFund planned operations throughConference callLive audio webcast scheduled todayBiopharma holdingsChief executive officerNew drug

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