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Acadia chief warns Trump 'most favoured nation' policy threatens global drug R&D partnerships

 The chief executive of Acadia Pharmaceuticals has warned that President Donald Trump's "most favoured nation" pricing policy risks undermining the international research collaborations that have underpinned drug discovery for decades, in the latest sign of mounting industry concern over the regulatory and commercial direction of US pharmaceutical policy.

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Nigeria's Neimeth posts strong Q1 revenue gains but debt costs cloud the recovery

Neimeth International Pharmaceuticals, one of Nigeria's longest-established drugmakers, posted strong revenue growth in the first quarter of 2026, continuing a turnaround that has lifted the Lagos-listed group out of three years of losses — even as escalating finance costs and an entrenched debt load underscore how challenging the operating environment remains for the country's pharmaceutical industry.

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Kazakhstan greenlights $80mn pharmaceutical plant in latest push for domestic drug self-sufficiency

Kazakhstan has approved an investment agreement underpinning a 42.5bn tenge (around $80mn) pharmaceutical production complex in the central region of Karaganda, in the latest step of a state-driven campaign to reduce the country's reliance on imported medicines and build a domestic manufacturing base in higher-value therapeutic categories.

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Rigel pays $85mn for global rights to first FDA-approved protein degrader in breast cancer

Rigel Pharmaceuticals has agreed to acquire exclusive global rights to Veppanu, the first FDA-approved therapy in a new class of cancer drugs that destroys disease-causing proteins rather than blocking them, paying $85mn upfront to Arvinas and Pfizer in a deal that materially repositions the South San Francisco-based group as a specialist commercial player in protein degradation oncology.

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Micro-cap Mira Pharmaceuticals publishes early data on obesity-and-addiction drug candidate

Mira Pharmaceuticals, a small US clinical-stage biotech, has published peer-reviewed preclinical data for its experimental oral drug candidate SKNY-1, a compound being developed simultaneously as a treatment for obesity and nicotine addiction — a dual ambition that reflects the growing biological convergence between metabolic and addiction medicine.

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GSK turns to Sino Biopharma to push hepatitis B 'functional cure' into Chinese market

GSK has struck an exclusive partnership with Hong Kong-listed Sino Biopharmaceutical to accelerate the launch of bepirovirsen, its closely watched experimental treatment for chronic hepatitis B, in mainland China — the largest single market for the disease and one of the most strategically significant geographies for what would be a first-in-class functional cure.

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Former Novartis Compliance Attorney Revives Whistleblower Claims in New Jersey Appeal

A New Jersey appeals court has revived whistleblower claims brought by a former compliance attorney at Novartis, reopening a case centred on alleged retaliation tied to internal compliance concerns.

The appellate court ruled that Cynthia Ham plausibly alleged a continuing pattern of retaliation under New Jersey’s Conscientious Employee Protection Act (CEPA), reversing an earlier decision that dismissed several claims as time-barred.

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D.C. Circuit Appears Sceptical of Teva Challenge in Medicare Drug Pricing Fight

A U.S. appeals court hearing over Medicare drug price negotiations has added to mounting pressure on pharmaceutical companies challenging the Inflation Reduction Act’s pricing regime.

During oral arguments before the D.C. Circuit, judges appeared sceptical of arguments brought by Teva Pharmaceuticals over how regulators classify medicines for Medicare price negotiations.

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Alto Neuroscience Pushes Back Against Investor Claims Over Depression Drug Trial

Alto Neuroscience is seeking to dismiss an investor lawsuit accusing the psychiatric biotech company of overstating the prospects of its lead depression drug candidate, Alto-100.

According to investors, the trial was negatively affected by patients who falsely reported taking the medication, raising questions about the reliability of the results and the company’s earlier public statements about the drug’s prospects.

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