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BioWorld - Tuesday, July 14, 2026
Home » Topics » Regulatory » FDA

FDA
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Ear, Nose and Throat

FDA awards rare pediatric disease designation to OTOF-GT for otoferlin gene-mediated hearing loss

Nov. 7, 2022
The FDA has awarded rare pediatric disease...
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Endocrine/Metabolic

FDA clears allogenic cellular therapy Allostem to enter clinic for type 1 diabetes

Nov. 4, 2022
Creative Medical Technology Holdings Inc. has received FDA clearance of its IND application for a clinical trial of Allostem in type 1 diabetes.
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Immuno-oncology

Omega's OTX-2002 awarded US orphan drug designation for HCC

Nov. 3, 2022
The FDA has awarded orphan drug designation to Omega Therapeutics Inc.'s OTX-2002, a first-in-class epigenomic controller engineered to downregulate c-Myc (MYC), for the treatment of hepatocellular carcinoma (HCC).
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Dermatologic

Brexogen receives FDA clearance for phase I trial of exosome-based therapy for atopic dermatitis

Nov. 3, 2022
The FDA has cleared Brexogen Inc. to initiate a phase I trial of BRE-AD01, an exosome-based therapy for atopic dermatitis.
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Endocrine/Metabolic

Eccogene cleared by FDA to begin phase I study of oral GLP-1 receptor agonist

Nov. 3, 2022
Eccogene (Shanghai) Co. Ltd. has received FDA clearance to begin a phase I study of its glucagon-like peptide 1 (GLP-1) receptor agonist ECC-5004 for type 2 diabetes.
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Cancer cells
Immuno-oncology

Turnstone receives IND clearance for phase I trial of TIDAL-01 for solid tumors

Nov. 2, 2022
Turnstone Biologics Corp. has received IND clearance from the FDA for the company's lead selected tumor-infiltrating lymphocyte (TIL) therapy program, TIDAL-01.
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Cancer

Abbisko cleared to enter clinic with FGFR inhibitor ABSK-121 for solid tumors

Nov. 2, 2022
Abbisko Therapeutics Co. Ltd. has received clearance from the FDA to initiate a phase I...
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FDA-approved-stamp4.png

October lags other months for FDA approvals and regulatory activity

Nov. 1, 2022
By Karen Carey
Despite a busy September, U.S. FDA approvals and global regulatory news fell in October to the lowest point this year. So far in 2022, the FDA has approved 127 drugs and biologics, including supplemental filings. This is 25% less than each of the last two years, which had 170 approvals in 2021 and 169 approvals in 2020 through the end of October. The last time approvals were lower than this year was 2016 when there were 121.
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US FDA updates its advice on expanded access

Nov. 1, 2022
By Mari Serebrov
Reflecting statutory and regulatory requirements added over the past five years, the U.S. FDA is issuing a revised draft question-and-answer (Q&A) guidance on expanded access to investigational drugs. One of several guidances recently issued, the 40-page draft incorporates requirements from the 21st Century Cures Act and the 2017 FDA Reauthorization Act that took effect after the current final Q&A guidance was updated in 2017. It also answers new questions sponsors have raised over the past few years.
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Patient receiving dialysis

FDA clears new tubing used in Fresenius hemodialysis machines

Oct. 31, 2022
By Mark McCarty
The U.S. FDA announced that it has cleared a new set of tubes used in hemodialysis machines made by Fresenius Medical Care AG & Co., of Bad Homburg, Germany, that are expected to overcome concerns about the previous tubes’ release of potentially toxic biphenyls. The agency acknowledged that it has no reports of adverse events related to the use of these chemicals in the silicone used to manufacture the tubes, stating that its action on this issue is driven solely by animal studies in the medical literature, none of which were cited in the FDA’s Oct. 28 announcement.
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