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Pharmaceutical Technology
2 小时
Stealth faces another hurdle as FDA delays decision on Barth syndrome drug
The FDA rejected the company’s initial NDA in 2021, citing the lack of an adequate trial to demonstrate efficacy.
Pharmaceutical Technology
1 小时
Podcast: Adaptive logistics in a changing clinical landscape
Adaptive logistics are vital for clinical trials, but there are challenges in navigating complexities of regulations and ...
Pharmaceutical Technology
2 小时
Emcure Pharmaceuticals opens new R&D centre in Gujarat, India
Emcure Pharmaceuticals has opened its new formulation research and development (R&D) centre at Ahmedabad, in the Indian state ...
Pharmaceutical Technology
3 小时
Bladder cancer: Shaping the future of global clinical trials
A new report dives into the evolving clinical trial landscape and transformative therapies changing lives for bladder cancer ...
Pharmaceutical Technology
3 小时
The $100bn frontier: Untapped potential in animal health innovation
There is no excerpt because this is a protected post. This content is password protected. To view it please enter your ...
Pharmaceutical Technology
5 小时
AbbVie and Neomorph link on oncology/immunology glue degraders
AbbVie and Neomorph are set to enter a partnership and option-to-license agreement to develop molecular glue degraders.
Pharmaceutical Technology
13 小时
Pharmaceutical Technology Excellence Awards 2024 – Winners Announced!
The Pharmaceutical Technology Excellence Awards winners have been announced! Download our full 50+ page report to find out ...
Pharmaceutical Technology
22 小时
FDA grants ODD status to Zai Lab’s lung cancer treatment
The FDA has granted orphan drug designation (ODD) to Zai Lab’s ZL-1310, aimed at treating small cell lung cancer (SCLC).
Pharmaceutical Technology
20 小时
Magazine: The biggest challenges clinical trials will face in 2025
The year ahead in clinical trials looks set to be one that is challenged and influenced by regulatory developments, new guidance, and broader political shifts.
Pharmaceutical Technology
21 小时
Biogen’s higher dose Spinraza under review by US and EU regulators
Biogen’s applications for the higher dose regimen of spinal muscular atrophy (SMA) drug Spinraza are now under review in the US and Europe.
Pharmaceutical Technology
1 天
Disc raises $225.5m as it eyes approval of rare skin disorder drug
Disc Medicine finalised the pivotal Phase III trial design of bitopertin in erythropoietic protoporphyria (EPP) with the FDA ...
Pharmaceutical Technology
1 天
FDA adds boxed warning to multiple sclerosis drugs after anaphylaxis cases
The FDA reported that six patients died after being injected with Teva’s Copaxone or Sandoz’s Glatopa. The US Food and Drug ...
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