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First in Human Dosed in Clinical Trial of ZMA001 for Treatment of Pulmonary Arterial Hypertension (PAH)

/PRNewswire/ Zymedi announced today that the first in human dosage of ZMA001, a monoclonal antibody being developed as a first-in-class treatment for.

South koreaInch on gwangyoksiSunghoon kimArss aminoacyl trna synthetasesPrnewswire zymediBlood instituteNational heartNational institutes of healthResearch development agreementPulmonary arterial hypertensionNational institutesCooperative researchDevelopment agreementMaximum tolerated dose

As cancer treatment advances, patients and doctors push back against drugs side effects

A cancer patient says,

Mount whitneyUnited statesLillian siuJulie gralowAlice shawJill feldmanPatricia lorussoChanapa tantibanchachaiLesley kailani glennTimothy yapAmerican society of clinical oncologyMd anderson cancer centerDrug administrationYale cancer centerPrincess margaret cancer centerPatient centred dosing initiative

Taysha Gene Therapies Announces First Pediatric Patient Dosed with TSHA-102 in REVEAL Phase 1/2 Pediatric Trial in Rett Syndrome

Initiation of REVEAL pediatric trial in the U.S.broadens the clinical evaluation of TSHA-102 to female patients 5-8 years old with stage three Ret.

United kingdomUnited statesUniversity medical centerElizabeth berry kravisSukumar nagendranCarolyn hawleyHayleigh collinsCompany contactExchange commissionTaysha gene therapies incHead of corporate communicationsCanale communicationsEuropean commissionRegulatory agencyUt southwestern gene therapy programUnited statesbroadens

Perspective Therapeutics Completes Initial Dose Escalation Cohort for Second Novel Targeted Alpha Therapy

SEATTLE, Nov. 16, 2023 Perspective Therapeutics, Inc. , today announced the completion of cohort 1 dosing in the Phase 1/2a clinical trial of [212Pb]VMT-α-NET in patients with unresectable or.

United statesMarkus puhlmannNikolaos trikalinosExchange commissionPerspective therapeutics incUniversity of iowaOncologist at washington university in stDepartment of energyChief medical officerMedical oncologistWashington universityMayo clinicMaximum tolerated doseMaximum feasible doseModified toxicity probability intervalPerspective therapeutic

OSE Immunotherapeutics Presents First Positive Clinical Results With its anti-PD1 OSE-279 in Advanced Solid Tumors

NANTES, France, October 16, 2023 Regulatory News: OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnemo: OSE) presented the first Phase 1/2 positive clinical results with high affinity anti-PD1 monoclonal antibody OSE-279 in advanced solid tumors at the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, held in Boston, MA (October 11 – 15, 2023 - Abstract number 35371, Poster C063).

United statesNicolas poirierSilvia comisInternational conference on molecularHead of clinical developmentVeloxis pharmaceuticals incBoehringer ingelheimRegulatory affairsNantes university hospitalRegulatory newsMolecular targetsCancer therapeuticsClinical developmentDisease control rateMaximum tolerated doseNon small cell lung cancer

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