REGENXBIO PRESENTS POSITIVE TWELVE-MONTH PIVOTAL DATA FROM PHASE I/II/III CAMPSIITE® TRIAL OF RGX-121 FOR TREATMENT OF MPS II
REGENXBIO INC - RGX-121 IMPROVES OUTCOMES FOR MPS II PATIENTS
REGENXBIO INC - PRIMARY ENDPOINT OF CSF HS D2S6 REDUCTION MET
REGENXBIO INC - FDA DECISION ON RGX-121 EXPECTED BY FEBRUARY 8, 2026
Source text: ID:nPn5glkbna
Further company coverage: RGNX.O
Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.