FDA
Entity.
- Evidence
- 3,442 documents · 277 separate publishers
- Standing
- A name from our starting list; its record is kept up to date automatically from coverage
- Time
- first seen 6 Apr 2026, last seen 11 Nov 2026
- Measured
- 36% of mentions say something specific about it; the rest only name it
- As of
- 11 Nov 2026
Where this comes from
- Tech Times · 2026-11-11 · PepGen's Myotonic Dystrophy Drug Sets Phase 2 Efficacy Record: FDA Hold Still Bars American Patients (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves pembrolizumab with chemoradiotherapy for FIGO 2014 Stage III-IVA cervical cancer (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves pembrolizumab as adjuvant treatment for non-small cell lung cancer (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves osimertinib with chemotherapy for EGFR-mutated non-small cell lung cancer (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves osimertinib for locally advanced, unresectable (stage III) non-small cell lung cancer following chemoradiation therapy (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves obecabtagene autoleucel for adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves nogapendekin alfa inbakicept-pmln for BCG-unresponsive non-muscle invasive bladder cancer (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves nivolumab in combination with cisplatin and gemcitabine for unresectable or metastatic urothelial carcinoma (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves nivolumab for adjuvant treatment of Stage IIB/C melanoma (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves nivolumab and hyaluronidase-nvhy for subcutaneous injection (opens the source in a new tab)
- FDA Drug News · 2026-11-10 · [APPROVAL] FDA approves new and updated indications for temozolomide under Project Renewal (opens the source in a new tab)
- Food Ingredients First · 2026-11-10 · US FDA revokes authorizations for solvent uses in natural food color manufacturing (opens the source in a new tab)
What is claimed about it
- Corroborated: Reported by three or more sources that did not copy each other.
- Reported by two: Reported by two sources that did not copy each other.
- Single source: Reported by one source so far.
- Could not check: We could not count this claim's sources, so we do not say how well it is supported.
- Novocure’s device for treating brain metastases rejected by FDA Single source · first reported 10 Nov 2026
- FDA orders class-wide GLP-1 label update to include potential risk for rare eye disease Corroborated · first reported 9 Nov 2026
- STAT+: FDA approves novel Bayer drug to reduce recurrence of stroke Reported by two · first reported 9 Nov 2026
- FDA Orders New Vision Loss Warning for Ozempic, Wegovy, Mounjaro and Zepbound Could not check · first reported 9 Nov 2026
- FDA grants accelerated approval to pirtobrutinib for chronic lymphocytic leukemia and small lymphocytic lymphoma Single source · first reported 9 Nov 2026
- FDA approves selpercatinib for locally advanced or metastatic RET fusion-positive solid tumors Single source · first reported 9 Nov 2026
- Samsung Bioepis Puts Keytruda Biosimilar Into FDA Review With Full Phase 3 Lung Cancer Trial Data Corroborated · first reported 7 Nov 2026
- FDA approves cosibelimab-ipdl for metastatic or locally advanced cutaneous squamous cell carcinoma Single source · first reported 7 Nov 2026
- FDA approves amivantamab-vmjw with carboplatin and pemetrexed for non-small cell lung cancer with EGFR exon 19 deletions or L858R mutations Single source · first reported 7 Nov 2026
- Lilly and Hims & Hers expand access to FDA-approved Lilly medicines Could not check · first reported 6 Nov 2026
- HUTCHMED (HCM) Secures Second FDA Orphan Drug Designation for Sovleplenib Targeting Autoimmune Hemolytic Anaemia Could not check · first reported 5 Nov 2026
- PulseAI Receives U.S. FDA 510(k) Clearance of AI-Powered Arrhythmia Analysis Model for Wearables Single source · first reported 5 Nov 2026