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Synageva was a rare disease-focused biotech company with multiple enzyme replacement therapy programs in development. The company's lead program, Kanuma (sebelipase alfa), was under Priority Review with the FDA and accelerated assessment with the EMA as of mid-2015, with regulatory decisions expected in the second half of 2015. The company's second program, SBC-103 for MPS IIIB, was in Phase 1/2 trials and had received Fast Track designation from the FDA in January 2015.
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