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Mashup Score: 11FDA Approves Trastuzumab Deruxtecan in HER2+ Solid Tumors - 1 month(s) ago
Fam-trastuzumab deruxtecan-nxki received accelerated approval from the FDA for adult patients with unresectable or metastatic HER2-positive solid tumors.
Source: www.targetedonc.comCategories: General Medicine News, Onc News and JournalsTweet
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Mashup Score: 1IND Application Submitted to FDA for SynKIR-310 Trial in R/R B-NHL - 1 month(s) ago
An investigational new drug application for SynKIR-310’s phase 1 trial targeting relapsed/refractory B-cell non-Hodgkin lymphomas was submitted to the FDA.
Source: www.targetedonc.comCategories: General Medicine News, Onc News and JournalsTweet
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Mashup Score: 3
With the FDA clearance of an investigational new drug application, a phase 1 clinical trial evaluating NST-628 will start in mid-2024.
Source: www.targetedonc.comCategories: General Medicine News, Onc News and JournalsTweet
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Mashup Score: 3
With the FDA clearance of an investigational new drug application, a phase 1 clinical trial evaluating NST-628 will start in mid-2024.
Source: www.targetedonc.comCategories: General Medicine News, Onc News and JournalsTweet
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Mashup Score: 0Patients With Esophageal Cancer Have ‘More Options’ With Tevimbra - 1 month(s) ago
The GI cancer space has “made huge strides” in recent years, which opened more options for patients with a type of esophageal cancer, an expert said.
Source: www.curetoday.comCategories: General Medicine News, NursingTweet
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Mashup Score: 1FDA Approves Safety Label Changes for Fluorouracil Injection - 2 month(s) ago
The FDA strengthened safety warnings for fluorouracil due to dihydropyrimidine dehydrogenase deficiency that can cause severe adverse effects.
Source: www.targetedonc.comCategories: General Medicine News, Onc News and JournalsTweet
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Mashup Score: 0FDA clears self-driving mobile C-arm from Siemens Healthineers - 2 month(s) ago
Siemens Healthineers announced today that the FDA granted clearance for its Ciartic Move mobile C-arm with self-driving capabilities.
Source: www.massdevice.comCategories: General Medicine News, General HCPsTweet
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Mashup Score: 0
The FDA has cleared Sequel’s twiist, a novel automated insulin delivery system, expanding patient choice for individuals with type 1 diabetes.
Source: www.hcplive.comCategories: General Medicine News, General HCPsTweet
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Mashup Score: 0Reacting to the FDA Approval of Fluticasone Propionate Nasal Spray, with James Palmer, MD - 2 month(s) ago
James Palmer, MD, provides perspective on the FDA’s decision to approve fluticasone propionate nasal spray for adults with chronic rhinosinusitis without nasal polyps.
Source: www.hcplive.comCategories: General Medicine News, General HCPsTweet
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Mashup Score: 4FDA Warns of T-Cell Malignancy Risk in CAR-T Immunotherapies | ASH Clinical News | American Society of Hematology - 2 month(s) ago
The U.S. Food and Drug Administration (FDA) issued a warning about the risk of T-cell malignancies in patients who have received BCMA- or CD19-directed autologous chimeric antigen receptor (CAR) T-cell immunotherapies. The warning followed the receipt of reports from clinical trials and post-marketing adverse event sources detailing T-cell malignancy occurrences in this patient population. A press release from the FDA noted that the benefits of these therapies still outweigh this risk, but the need for
Source: ashpublications.orgCategories: General Medicine News, Hem/OncsTweet
BREAKING: The #FDA granted accelerated approval to T-DXd in HER2-positive tumors that are unresectable or metastatic that have been treated with prior systemic treatment. https://t.co/azi8TunkrB