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BioWorld - Thursday, April 2, 2026
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Regulatory
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Regulatory actions for May 4, 2021

May 4, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Biobeat, Lifespine, Purigen, Santen, Standard Bariatrics.
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Regulatory actions for May 4, 2021

May 4, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astellas, Carmot, Clarity, Eli Lilly, Hutchmed, Immunomet, Newron, Pfizer, Quercis, R-Pharm Germany, Siga Technologies, Viiv Healthcare.
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Molli Surgical magnetic breast tumor marking device

FDA clears Molli Surgical’s magnetic breast tumor marking device

May 3, 2021
By Meg Bryant
Molli Surgical Inc. has won the FDA’s nod for its wire-free localization technology for breast cancer surgery. The company said the Molli system helps radiologists tag cancerous lesions quickly and precisely, facilitating surgical excision and eliminating a source of anxiety associated with breast tumor removal.
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Continuing accelerated approvals can be problematic

May 3, 2021
By Mari Serebrov
While last week’s marathon Oncologic Drugs Advisory Committee meeting to consider accelerated approvals for cancer drugs that didn’t demonstrate effectiveness in confirmatory trials was a good step forward, oncologists need the FDA to do more to ensure drug labeling truly reflects the benefit of the product.
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Gavel and block with Chinese flag

China overhauls patent law to stay competitive in biotech innovation

May 3, 2021
By Elise Mak
To honor its part for phase one of the U.S.-China trade deal, China has revised its patent law to establish a drug patent linkage system and provide compensation for lost patent terms, similar to procedures under the U.S. Hatch-Waxman Act. Effective June 1, the new patent law is expected to drive biotech innovation and welcome more foreign drugs to the China market.
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Biotech first: EC fines company over M&A divestiture info

May 3, 2021
By Mari Serebrov
In a first for the biotech industry, the European Commission (EC) has imposed a €7.5 million (US$9.05 million) fine on Sigma-Aldrich, under the EU’s 2004 Merger Regulation, for providing incorrect or misleading information during a merger investigation.
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T2D or not T2D: Astrazeneca’s Farxiga gets yes answer to CKD question as class grows

May 3, 2021
By Randy Osborne
Astrazeneca plc followed up its win a year ago in heart failure (HF) with yet another approval for its oral  SGLT2 inhibitor, Farxiga (dapagliflozin), now cleared by the FDA to reduce the odds of kidney function decline, failure, cardiovascular death and hospitalization for HF in adults with chronic kidney disease (CKD) at risk of disease progression. 
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Regulatory actions for May 3, 2021

May 3, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Medtronic plc., Molli Surgical.
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Regulatory actions for May 3, 2021

May 3, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Advicenne, Amicus, Avrobio, Astrazeneca, Camurus, Chiesi, Clearside, Galmed, Intra-Cellular, Jacobio, Moderna.
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FDA approves Farxiga for chronic kidney disease

May 3, 2021
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