EuroBiotech Report—Nanobiotix soars, Novo backs NDE, Boehringer expansion, Summit and EMA-Amicus | Bio Tech

Welcome to the latest edition of our weekly EuroBiotech Report. We start this week with Nanobiotix, which saw its stock soar after reporting phase 2/3 soft tissue sarcoma data. Novo Holdings invested CHF 20 million ($20 million) in NBE Therapeutics. Boehringer Ingelheim unveiled a €230 million investment in a German biologics center. Summit Therapeutics dumped its Duchenne muscular dystrophy drug following a midphase failure. The EMA told Amicus Therapeutics to generate more data before filing for conditional approval. And more.Nick Taylor  

1. Nanobiotix soars as late-phase cancer trial hits endpoint

A phase 2/3 trial of Nanobiotix’s NBTXR3 in soft tissue sarcoma has met (PDF) its primary endpoint. The top-line success against the pathological complete response rate endpoint sent Nanobiotix’s stock up by more than 50%.

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2. ADC startup NBE raises $20M from Novo Holdings, doubling size of Boehringer-backed B round

Novo Holdings has invested CHF 20 million ($20 million) in NBE Therapeutics, doubling the size of the startup’s series B round. NBE will use the money to start testing anti-ROR1 antibody-drug conjugate (ADC) NBE-002 in solid tumor patients.

3. Boehringer commits €230M to build German biologics center

Boehringer Ingelheim has unveiled a €230 million ($268 million) investment in its biologics capacity. The investment will support the construction of a biologics development center at Boehringer’s R&D site in Biberach, Germany.

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4. Summit dumps ezutromid after phase 2 Duchenne fail

Despite putting up encouraging early data, Summit Therapeutics’ Duchenne muscular dystrophy (DMD) drug missed its primary and secondary endpoints in a phase 2 trial, leading the biotech to drop the program and focus its energies behind its antibiotic pipeline. 

5. EMA demands more data from Amicus, denting stock

The EMA has told Amicus Therapeutics it lacks the data to file for conditional approval of its Pompe disease drug in Europe. Amicus needs to gather data on more patients and track the progress of previously treated people before seeking conditional approval, delaying the filing to 2019 or beyond.

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