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Chiasma Looks Ahead To First Approval With "Revolutionary" Technology Opportunity

Anticipating an April 15 user fee date for oral ocreotide for acromegaly, Chiasma thinks its platform technology to make peptides orally available can offer substantial opportunities for therapeutic optionality.

With an FDA action date just around the corner for Mycapssa, its oral reformulation of ocreotide, a peptide somatostatin analog used for acromegaly, Chiasma Inc. believes it is positioned to offer potential partners a paradigm-changing technology for providing oral therapeutic options with peptides currently available only as injectable therapies.

Mycapssa is a reformulation of Novartis AG's Sandostatin, which originally had to be injected subcutaneously three times a day

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