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Hoth Therapeutics: FDA Grants Pre-IND Meeting For HT-KIT; Stock Surges

Hoth Therapeutics, Inc. (HOTH) announced the Pre-IND meeting previously requested for HT-KIT with the FDA has been granted to receive written responses only from the FDA that are targeted for delivery on November 7, 2023.

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FDA Grants First Marketing Authorization for a DNA Test to Assess Predisposition for Dozens of Cancer Types

The U.S. Food and Drug Administration granted de novo marketing authorization for the Invitae Common Hereditary Cancers Panel, an in vitro diagnostic test that can help detect hundreds of genetic variants associated with an elevated risk of developing certain cancers. The test can also help identify potentially cancer-associated hereditary variants in individuals with already-diagnosed cancer. The test, which is the first of its kind to be granted FDA marketing authorization, evaluates DNA.

United statesJeff shurenRadiological healthDrug administrationUs department of healthCenters for diseaseHuman servicesInvitae common hereditary cancers panelFirst marketing authorizationAssess predispositionDisease controlPeutz jeghers syndromePress release imageCancer associatedLready diagnosedPress release

First Blood Test for Dozens of Hereditary Cancers Approved by FDA

First Blood Test for Dozens of Hereditary Cancers Approved by FDA
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United statesJeff shurenUniversity of vermont medical centerInvitae common hereditary cancers panelCenters for diseaseRadiological healthDisease controlVermont medical centerPeutz jeghers syndrome

FDA Grants Marketing Authorization to First DNA Test to Assess Genetic Predisposition to Select Cancers

The FDA has granted de novo marketing authorization for the Invitae Common Hereditary Cancers Panel, an in vitro diagnostic test designed to detect genetic variants associated with an elevated risk of developing certain types of cancer.

Jeff shurenInvitae common hereditary cancers panelRadiological healthPrecision medicine in oncology

Why Invitae Stock Popped Today | The Motley Fool

Invitae just received a key marketing authorization from the FDA for a first-of-its-kind cancer test.

United statesKen knightDrug administrationInvitae common hereditary cancers panel

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