Sarepta Dmd Clinical Hold at Olivia Quinn blog

Sarepta Dmd Clinical Hold. Sarepta therapeutics has successfully defused concerns about a fda clinical hold on one of its duchenne muscular dystrophy. Sarepta therapeutics has announced new data from part b of its phase 2 momentum study (nct04004065) with results showing that treatment with srp. Two months after sarepta was hit with a clinical hold by the fda, the rare disease biotech has seen this lifted after sorting out a quality blip. Sarepta therapeutics has broken free from an fda hold—put in place this june—on its phase 2 duchenne muscular dystrophy (dmd) clinical trial.

Sarepta Talks Progress, Plans for DMD Gene Therapy Trials for SRP9001
from musculardystrophynews.com

Sarepta therapeutics has broken free from an fda hold—put in place this june—on its phase 2 duchenne muscular dystrophy (dmd) clinical trial. Two months after sarepta was hit with a clinical hold by the fda, the rare disease biotech has seen this lifted after sorting out a quality blip. Sarepta therapeutics has announced new data from part b of its phase 2 momentum study (nct04004065) with results showing that treatment with srp. Sarepta therapeutics has successfully defused concerns about a fda clinical hold on one of its duchenne muscular dystrophy.

Sarepta Talks Progress, Plans for DMD Gene Therapy Trials for SRP9001

Sarepta Dmd Clinical Hold Sarepta therapeutics has announced new data from part b of its phase 2 momentum study (nct04004065) with results showing that treatment with srp. Two months after sarepta was hit with a clinical hold by the fda, the rare disease biotech has seen this lifted after sorting out a quality blip. Sarepta therapeutics has broken free from an fda hold—put in place this june—on its phase 2 duchenne muscular dystrophy (dmd) clinical trial. Sarepta therapeutics has announced new data from part b of its phase 2 momentum study (nct04004065) with results showing that treatment with srp. Sarepta therapeutics has successfully defused concerns about a fda clinical hold on one of its duchenne muscular dystrophy.

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