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BioWorld - Tuesday, February 17, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

March 16, 2016

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GI Dynamics misses safety, efficacy endpoints in Endobarrier trial

GI Dynamics Inc. continues to face stumbling blocks in its bid to obtain FDA approval for its endoscopically-delivered device therapy for the treatment of Type 2 diabetes and obesity. The Lexington, Mass-.based company said on Tuesday, that its Endobarrier device failed to meet safety and efficacy endpoints in the ENDO pivotal trial, but noted it would still continue to move forward with plans to gain FDA approval. Read More

Industry lowers MDUFA demands in effort to cap user fee funding

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Roche deal pumps up Cellnovo prospects for insulin delivery

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EMCDD: Working at the edges of fluorescence-guided surgery

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Panel gives Abbott's Absorb the nod in landslide vote

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India's device sector could be worth $17.6 billion by 2020

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Other news to note

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Financings

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Appointments and advancements

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Product briefs

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MDD's Oncology Extra

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