Synageva BioPharma announces positive results from Phase I/II trial of SBC-102

theflyonthewall.com

Synageva BioPharma announced encouraging safety and tolerability data as well as effects consistent with preclinical findings and known mechanism of action. Patients from this 4-week Phase I/II trial of SBC-102 in adults with late onset LAL Deficiency continue to transition into an open-label extension study.

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