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Candel Therapeutics (CADL) Granted FDA Orphan Drug Designation for CAN-3110

Candel Therapeutics (CADL) Granted FDA Orphan Drug Designation for CAN-3110
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E antonio chioccaDrug administrationCandel therapeutics incDepartment of neurosurgery at brighamProfessor at harvard medical schoolCancer foundationCandel therapeuticsOrphan drug designationFast track designationBreak through cancer foundationTrack designationPaul peter takChief executive officerAntonio chioccaHarvard medical schoolPrincipal investigator

JJP Biologics Announces Positive Decision to Execute a First-in-Human Clinical Trial of Anti-Inflammatory mAb JJP-1212 (anti-CD89)

JJP Biologics has received a positive conclusion on the Clinical Trial Application assessment for a Phase I Study of a potential first-in-class anti-CD89 antagonist, JJP-1212 monoclonal antibody for

Haute normandieMarjolein van egmondDawid lyzwaPascal jolyPawel szczepanskiEuropean unionEuropean medicines agencyVu university medical center amsterdamRouen university hospitalResearch agency noHead of clinical developmentUniversity medical center regensburgEuropean commissionResearch agencyClinical trial applicationPhasei study

JJP Biologics Announces Positive Decision to Execute a FirstinHuman Clinical Trial of AntiInflammatory mAb JJP1212 antiCD89

JJP Biologics a private biopharmaceutical company developing innovative antibodybased therapies announces a positive decision issued by the European Medicines Agency on the Clinical Trial Application to conduct a phase I clinical study in healthy participants EudraCT 20235086613300 with their potential firstinclass antiCD89 antagonist JJP1212.

Haute normandiePascal jolyMarjolein van egmondResearch agencyEuropean unionEuropean commissionHead of clinical developmentUniversity medical center regensburgEuropean medicines agencyResearch agency noVu university medical center amsterdamRouen university hospitalClinical trial applicationMedical center amsterdamScientific advisory boardManagement board member

VBI Vaccines Announces New Tumor Response Data from Ongoing Randomized Controlled Phase 2b Study of VBI-1901 in Recurrent Glioblastoma Patients

Among the 7 patients on VBI-1901 treatment long enough to have 1+ MRI scan at the time of analysis, one partial tumor response and two stable disease observations have occurred as of May 15,.

United kingdomUnited statesPrehevbrio prehevbriBrii biosciencesDavide andersonJeff baxterCompany quarterly reports on formAmerican society of clinical oncologyVaccines incOncology centerDrug administrationClinical oncologyAnnual meetingScientific officerFast trackOrphan drug designations

NurExone Reports First Quarter 2024 Financial Results and Provides Corporate Update, moving forward with FDA guidelines for the Human Trials

NurExone Reports First Quarter 2024 Financial Results and Provides Corporate Update, moving forward with FDA guidelines for the Human Trials
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United statesNew yorkLior shaltielEva reuterJoe oconnorJoe oliverBarbara shecterJustin trudeauRam petterChrystia freelandGabriel friedmanContract research organizationCompany or nurexoneCompany annual information formParliament hillPostmedia network inc