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INOVIO Announces FDA's Orphan Drug Designation For INO-3107 - Quick Facts

(RTTNews) - INOVIO (INO) said the FDA granted orphan drug designation for INO-3107, the company's DNA medicine being evaluated in a Phase 1/2 trial for treatment of recurrent respiratory papillomatosis.

The open-label, multicenter INO-3107 Phase 1/2 trial is currently open to enrollment to recruit 63 subjects in the U.S. and will evaluate the efficacy, safety, tolerability, and immunogenicity of INO-3107 in subjects with HPV 6 and/or 11-associated recurrent respiratory papillomatosis who have required at least two surgical interventions per year for the past three years for the removal of associated papilloma.

The views and opinions expressed herein are the views and opinions of the author and do not necessarily reflect those of Nasdaq, Inc.

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