Snapshot from Jun 25, 2026 at 22:38 UTC. For live data and tracking: View Live
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Guardant360 CDx

Tracked across 1 events · 7 articles · First seen Jun 11, 2026 · Last active Jun 11, 2026

Sentiment
75
Attention
4
Events
1
Relationships
0
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4 75
Regulatory
The United States — Food and Drug Administration (FDA) has approved Guardant360 CDx, a liquid biopsy test developed by Guardant Health, as a companion diagnostic for Boehringer Ingelheim's HERNEXEOS (zongertinib tablets). HERNEXEOS is the first…
Impact: Guardant360 CDx received FDA approval as a companion diagnostic for HERNEXEOS, expanding its indications and reinforcing its role in personalized lung cancer care. This approval is the 27th CDx indication for the test.
Jun 11, 2026 · 7 articles
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