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BioWorld - Saturday, January 10, 2026
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Regulatory, BioWorld
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Regulatory actions for June 22, 2023

June 22, 2023
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acelink, Biocardia, Bluebird, Calliditas, Cormedix, Diamedica, Jadeite, Teikoku, Xbrane.
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PhRMA suit: IRA negotiations also a ‘taking’ from patients, providers

June 21, 2023
By Mari Serebrov
The floodgates have opened for challenges to the new U.S. drug price negotiation process laid out in the Inflation Reduction Act (IRA) that was narrowly passed last year.
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China greenlights Salubris’ HIF-PH inhibitor for anemia

June 21, 2023
By Doris Yu
Shenzhen Salubris Pharmaceuticals Co. Ltd. received marketing approval from China’s NMPA for enarodustat as a treatment for anemic patients with chronic kidney disease (CKD) that are not on dialysis.
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SK Bioscience strives for ‘equal access’ to Korean COVID-19 vaccine with WHO approval

June 21, 2023
By Marian (YoonJee) Chu
The World Health Organization (WHO) recently gave an emergency use listing (EUL) for SK Bioscience Ltd.’s COVID-19 vaccine called Skycovione, a self-assembled nanoparticle vaccine that targets the SARS-CoV-2 spike protein.
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Eye and financial charts

No studies, no data, no approval: Aldeyra gets a CRL

June 21, 2023
By Lee Landenberger
In its newly issued complete response letter (CRL) to Aldeyra Therapeutics Inc., the U.S. FDA said there’s just not enough evidence of efficacy right now to approve ADX-2191, an injectable vitreous-compatible formulation of methotrexate to treat primary vitreoretinal lymphoma (PVRL).
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Vyvgart Hytrulo wins U.S. FDA approval for generalized myasthenia gravis

June 21, 2023
By Karen Carey
Following a three-month delay, the U.S. FDA approved under priority review a subcutaneous formulation of Argenx SE’s efgartigimod, offering patients a much more convenient way to treat generalized myasthenia gravis (gMG).
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Regulatory actions for June 21, 2023

June 21, 2023
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aardvark, Advantage, Agepha, Akebia, Aldeyra, Amarin, Amgen, Arcellx, Argenx, Aridis, ARS, Biologix, Boehringer Ingelheim, Geron, Pfizer, Precigen, Replay, Sonnet.
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IRA pile-on expands with third challenge

June 20, 2023
By Mari Serebrov
Bristol Meyers Squibb Co. (BMS) joined the Inflation Reduction Act (IRA) pile-on June 16, filing a third constitutional challenge to the U.S. Medicare drug price negotiations mandated in the law that was narrowly passed last year on a partisan vote.
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Arcellx CAR T-cell therapy grinds to halt as FDA reacts to patient death

June 20, 2023
By Caroline Richards
Following the death of a patient, the U.S. FDA halted Arcellx Inc.’s phase II pivotal trial of its CAR T-cell therapy for relapsed or refractory multiple myeloma (MM), putting Gilead Sciences Inc., which in December made the risky decision to part with $225 million up front for rights to the immunotherapy, in likely turmoil.
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Regulatory actions for June 20, 2023

June 20, 2023
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: F2G, Freya, Iaso, Sirnaomics, SK.
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