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HOOKIPA Pharma Announces Positive Clinical Data to be Presented at the American Society for Clinical Oncology 2024 Annual Meeting

HOOKIPA to present an oral abstract at the American Society for Clinical Oncology 2024 Annual Meeting on June 4Updated data of HB-200 plus pembrolizumab demonstrate a favorable safety profile and.

United statesJoern aldagExchange commissionDrug administrationUniversity of chicago department medicineEuropean medicines agencyPharma incAmerican society for clinical oncologyUniversity of chicago medicineAmerican societyClinical oncologyNeck oral abstract sessionChief executive officerInvestigator initiated trialSari rosenbergChicago department

NeuroSense Vice President of R&D Shiran Zimri, Ph D to Participate in the 3rd Annual ALS Drug Development Summit

NeuroSense Vice President of R&D Shiran Zimri, Ph D to Participate in the 3rd Annual ALS Drug Development Summit
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United kingdomUnited statesShiran zimriDrug development summitNeurosense therapeutics ltdExchange commissionEuropean medicines agencyExchange commission onDrug administrationNeurosense therapeuticsVice presidentDevelopment summitCombination therapyLatest progressDiscovery summitRating scale revised

Ractigen Therapeutics Receives IND Approval from China s NMPA to Initiate Phase 1 Clinical Trials for RAG-17 in SOD1-ALS Patients

Ractigen Therapeutics Receives IND Approval from China s NMPA to Initiate Phase 1 Clinical Trials for RAG-17 in SOD1-ALS Patients
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Cheng liChina national medical products administrationDrug administrationDrug evaluationNational medical products administrationInvestigational new drugAmyotrophic lateral sclerosisSuperoxide dismutaseLei caiOrphan drug designationInvestigator initiated trial

NeuroSense Announces New Positive Data Analysis from PARADIGM Clinical Trial Demonstrating Statistically Significant Slowing of Disease Progression in High-Risk ALS Patients

NeuroSense Announces New Positive Data Analysis from PARADIGM Clinical Trial Demonstrating Statistically Significant Slowing of Disease Progression in High-Risk ALS Patients
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United kingdomUnited statesJeremym shefnerBarrow neurological instituteDrug administrationNeurosense therapeutics ltdEuropean medicines agencyPrnewswire neurosense therapeutics ltdEuropean network for the cureSense therapeuticsConfidence intervalEuropean networkRisk factorSeeing primecRating scale revisedInvestigator initiated trial

Biodexa Pharmaceuticals PLC: Preliminary Results for the Year Ended 31 December 2023

Biodexa Pharmaceuticals PLC: Preliminary Results for the Year Ended 31 December 2023
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United statesUnited kingdomSan franciscoRussian federationStephen parkerDennis riedlMonte carloSimon turtonActa neuropatholBiosciences incCompany issued ordinaryColumbia universityUniversity of albertaAdss of the companyUniversity of texasArmistice capital master fund ltd