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Gene Editing for Huntington s Disease Shows Promise in Pigs

Gene Editing for Huntington s Disease Shows Promise in Pigs
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New yorkUnited statesSan franciscoLiangxue laiMadolyn bowman rogersShihua liOlivier danosClaire clellandUniversity of californiaSen yan at jinan universityJinan universityChinese academy of sciencesBiomedical engineeringChinese academyNew york citySen yan

Coave Therapeutics Strengthens Board of Directors

- Frederic Chereau named Chairman of the Board - Seasoned entrepreneur, Dr Claudia Mitchell, appointed Non-executive Director PARIS, Oct. 20, 2022 /PRNewswire/ Coave Therapeutics

United statesFrance generalHaute normandieFranche comtérEleanor perkinOlivier danosWillem broekaertSylvie berrebiBruno montanariClaudia mitchellKostenloser wertpapierhandelAstellas pharmaThierry laugelGuillaume blavierFrederic chereauPhilippe monteyne

Coave Therapeutics Announces Formation of Scientific Advisory Board to Drive its Pipeline Strategy for Next-generation Gene Therapies Targeting CNS Diseases

/PRNewswire/ Coave Therapeutics ( Coave ), a clinical-stage biotechnology company focused on developing life-changing gene therapies for CNS (Central.

United statesFrance generalFranche comtérEleanor perkinOlivier danosMark richardsonSylvie berrebiCharlesa pappasErwan bezardDavid standaertAnthony schapiraStephane palfiThomas gasserThomas blaettlerJohnn whitakerLamya shihabuddin

REGENXBIO Announces FDA Clearance of IND for Clinical Trial of RGX-202, a Novel Gene Therapy Candidate for Duchenne Muscular Dystrophy

/PRNewswire/ Potential one-time gene therapy for the treatment of Duchenne includes a novel, optimized microdystrophin transgene and REGENXBIO s proprietary.

United statesDavid rosenOlivier danosBrendan burnsTricia truehartExchange commissionCorporate communicationsTechnology platformTechnology platform licenseesSecurities exchangeDrug administrationInvestigational new drugUnited states foodChief scientific officerNorth star ambulatory assessmentChief executive officer

REGENXBIO Announces FDA Clearance of IND for Clinical Trial of RGX-202, a Novel Gene Therapy Candidate for Duchenne Muscular Dystrophy

/PRNewswire/ Potential one-time gene therapy for the treatment of Duchenne includes a novel, optimized microdystrophin transgene and REGENXBIO s proprietary.

United statesDavid rosenOlivier danosBrendan burnsTricia truehartExchange commissionCorporate communicationsTechnology platformTechnology platform licenseesSecurities exchangeDrug administrationInvestigational new drugUnited states foodChief scientific officerNorth star ambulatory assessmentChief executive officer

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