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BioWorld - Wednesday, December 31, 2025
Home » Topics » Europe, BioWorld

Europe, BioWorld
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Positive Duchenne data for Santhera, confirmatory miss for Sarepta

Nov. 4, 2025
By Nuala Moran
No Comments
Five-year follow-up data for Santhera Pharmaceuticals AG’s Duchenne muscular dystrophy (DMD) drug, Agamree (vamorolone), confirm that its efficacy in preserving muscle function is comparable to standard-of-care corticosteroids, but that the overall side-effect profile is more benign. There was less positive DMD news from Sarepta Therapeutics Inc.
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U.K. flag on stethoscope

UK MHRA sets out reforms to speed rare disease therapy approvals

Nov. 3, 2025
By Nuala Moran
No Comments
The U.K. Medicines and Healthcare products Agency (MHRA) has committed to major reforms of how it regulates drugs for rare diseases, making it easier to run clinical trials and get approvals. The new rules will be published in full early in 2026 and come into effect later in the year, but following consultation with industry, academics and patients’ groups, the agency has released a position paper setting out its plans.
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Pfizer headquarters

Pfizer files two lawsuits to stop Novo's $9B buyout of Metsera

Nov. 3, 2025
By Nuala Moran
No Comments
Pfizer Inc. has delivered on its threat of legal action against the attempt by Novo Nordisk A/S to scupper its acquisition of Metsera Inc., and has filed two lawsuits, one alleging breach of contract, and a second claiming that a merger of Novo Nordisk and Metsera would violate antitrust regulations.
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Neurons

Uniqure HD gene therapy walloped by FDA opinion shift

Nov. 3, 2025
By Randy Osborne
No Comments
Uniqure NV is regrouping after a surprise switcheroo by the havoc-beset U.S. FDA regarding phase I/II studies with AMT-130 vs. external control in Huntington’s disease (HD) – news of which pushed down the Lexington, Mass.-based firm’s shares (NASDAQ:QURE) Nov. 3 by $33.40, a loss of 49%, at the closing price of $34.29.
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Vesper's oral frontotemporal dementia drug positive in phase Ib/II

Oct. 31, 2025
By Nuala Moran
No Comments
Neurodegeneration specialist Vesper Bio ApS has announced positive results from the phase Ib/II trial of its oral sortilin inhibitor VES-001 in frontotemporal dementia. The small study involved six participants who had not progressed to symptomatic disease but were carriers of mutations in the GRN gene that codes for progranulin, a growth factor that is essential for neuronal health.
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Three red darts on target

Novo Nordisk makes $9B counterbid for obesity specialist Metsera

Oct. 30, 2025
By Nuala Moran
No Comments
Pfizer Inc. is threatening legal action at an attempt by Novo Nordisk A/S to scupper its acquisition of Metsera Inc., with an unsolicited $9 billion offer for the anti-obesity specialist. That trumps Pfizer’s agreed bid made in September, which valued New York-based Metsera at $7.3 billion.
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Handshake with charts, maps, data

Qyuns and Roche partner in $1B+ bispecific antibody deal

Oct. 29, 2025
By Marian (YoonJee) Chu
No Comments
Qyuns Therapeutics Co. Ltd. signed a potential $1.07 billion license deal with Roche Holding AG, granting the latter exclusive rights to QX-031N – a human thymic stromal lymphopoietin and interleukin-33)-targeting bispecific antibody.
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Drug capsule spilling onto brain

Angelini signs $550M deal for Sovargen’s ASO drug in epilepsy

Oct. 29, 2025
By Marian (YoonJee) Chu
No Comments
Sovargen Co. Ltd. inked a $550 million license deal with Angelini Pharma SpA, granting Angelini development and commercialization rights to SVG-105, a novel antisense oligonucleotide drug candidate in preclinical development as a potential treatment for intractable epilepsy.
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Illustration of leg anatomy with target around knee

Levicept data show neurotrophin inhibitor may be disease modifying in osteoarthritis

Oct. 28, 2025
By Nuala Moran
No Comments
An examination of X-ray and MRI scans of 518 patients before and after treatment with Levicept Ltd.’s Levi-04 has shown that, in addition to providing significant analgesia, the selective neurotrophin-3 inhibitor may have a disease-modifying effect in osteoarthritis of the knee.
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Roctavian

Roc in hard place: Biomarin plans divestment to ratchet up numbers

Oct. 28, 2025
By Lee Landenberger
No Comments
Biomarin Pharmaceutical Inc. plans to divest its pioneering gene therapy for hemophilia, Roctavian (valoctocogene roxaparvovec), and remove what had been considered a potential blockbuster from the portfolio in order to grow the company.
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