Guardant Health's Guardant360 CDx approved for HER2-mutant NSCLC
The FDA cleared it as a companion diagnostic for Boehringer Ingelheim's targeted therapy as initial treatment.
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Blood-based precision oncology company
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In short: Guardant Health achieved several FDA approvals and guideline inclusions while facing an $83 million patent litigation loss.
The FDA cleared it as a companion diagnostic for Boehringer Ingelheim's targeted therapy as initial treatment.
The initiative aims to keep candidates informed about purpose-driven opportunities and advance the mission to conquer cancer.
The abstracts highlight methylation-based tumor classification, liquid biopsy advances, and the InfinityAI platform’s expanding clinical utility.
The ACS lists Shield™ as a blood-based colorectal screening option, noting it can expand access and help reach over 50 million unscreened Americans.
The FDA has approved the new Guardant360 Liquid CDx, an updated blood-based cancer test designed to support treatment selection in patients with advanced cancer, according...
Guardant Health Inc. failed to overturn an $83.4 million DNA-sequencing patent verdict and must pay a 6% ongoing royalty to TwinStrand Biosciences Inc. and the...
Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, today announced that the U.S. Food and Drug Administration (FDA) has approved Guard...
Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, announced that its FDA-approved Shield™ blood test is now included in updated Ameri...
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