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BioWorld - Tuesday, April 21, 2026
Home » Topics » Regulatory

Regulatory
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Multiple myeloma cells in the bone marrow.
Immuno-oncology

Trispecific antibody SIM-0500 approved for trials in the US and China for multiple myeloma

March 12, 2024
Simcere Zaiming, a subsidiary of Simcere Pharmaceutical Group Ltd., has received approval from the FDA and China’s National Medical Products Administration (NMPA) to conduct clinical trials with SIM-0500 in patients with relapsed or refractory multiple myeloma.
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Cancer cells
Cancer

Aprea’s WEE1 inhibitor set to enter phase I for cyclin E-overexpressing cancers

March 12, 2024
Aprea Therapeutics Inc. has received FDA clearance of its IND application for APR-1051, a next-generation inhibitor of WEE1 kinase.
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Test tubes, dropper and capsules
Cancer

Eilean Therapeutics’ menin inhibitor cleared for first-in-human study in Australia

March 12, 2024
Eilean Therapeutics LLC has announced clearance by the Human Research Ethics Committee in Australia for a first-in-human phase I trial of balamenib (ZE63-0302), an oral small-molecule inhibitor of the menin-KMT2A interaction.
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US FDA includes amyloid in revised Alzheimer’s draft

March 11, 2024
By Mari Serebrov
Reflecting the evolving scientific understanding of Alzheimer’s disease, the U.S. FDA revised its 2018 draft guidance on developing drugs to treat early Alzheimer’s.
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Celltrion files for US approval of Xolair biosimilar, CT-P39

March 11, 2024
By Marian (YoonJee) Chu
South Korean biopharmaceutical company Celltrion Inc. submitted a BLA to the U.S. FDA on March 10 to gain approval for its Xolair (omalizumab; Novartis AG) biosimilar, CT-P39, across major indications of asthma, food allergy and chronic spontaneous urticaria.
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Global market charts
2024 IMDRF Annual Meeting

Regulatory reliance emphasized at IMDRF meeting

March 11, 2024
By Mark McCarty
This year’s annual meeting of the International Medical Device Regulators Forum (IMDRF) revolves around regulatory reliance, a notion that approaches but does not quite stray into the realm of the mutual recognition agreement.
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Gavel and scales

US DOJ sets more aggressive course for enforcement activity

March 11, 2024
By Mark McCarty
U.S. deputy attorney general Lisa Monaco recently outlined some new programs related to federal enforcement across the economy, including some novel elements related to artificial intelligence (AI).
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FDA icons and doctor

‘Unexpected’ adcom to delay Lilly’s donanemab in Alzheimer’s

March 8, 2024
By Jennifer Boggs
A first-quarter 2024 launch for Alzheimer’s drug donanemab appears to be off the table as Eli Lilly and Co. disclosed a last-minute decision by the U.S. FDA to convene an advisory committee to review data from the phase III Trailblazer-ALZ 2 trial.
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Biden: US drug prices ‘wrong and I’m ending it’

March 8, 2024
By Mari Serebrov
In what was more of a campaign speech accompanied by frequent chants of “four more years,” U.S. President Joe Biden loaded the annual State of the Union address March 7 with what sounded like campaign promises for a second term. Among those promises were calls to Congress to expand the prescription drug price provisions of the 2022 Inflation Reduction Act.
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China and U.S. flags

Stuff of ‘science fiction’ driving US-China biotech race

March 7, 2024
By Mari Serebrov
Superhuman soldiers. Designer babies. Genetically tailored weapons. Mind-control. A foreign database containing the DNA of every person on the planet. The list reads like the plot of a science fiction horror story, but there’s no fiction involved. These are real threats from China raised by members of the U.S. House Select Committee on the CCP (Chinese Communist Party) at a March 7 hearing on the growing stakes of the bioeconomy and American national security.
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