Biopharma Transcript

Fulgent Genetics, Inc. FLGT

Nasdaq · Phase 2 · oncology · small molecule · EDGAR · Updated Nov 6, 2026

Fulgent Genetics, Inc. (Nasdaq: FLGT) is an oncology drug developer. Its lead program, FID-007, is in Phase 2 for cancers (broad range). Its next catalyst on record is FID-007: continued development efforts following end of Phase 2 meetings with FDA (date not stated).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: FID-007 — continued development efforts following end of Phase 2 meetings with FDA (date not stated). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
FID-007cancerssmall moleculePhase 2
FID-022cancerssmall moleculePhase 1
pre-clinical programscancers (various)small moleculePre-clinical

Recent results and decisions

  1. Nov 5, 2026
    started FID-022 first-in-human dose escalation study is ongoing, with dosing completed for the first four dose levels and maximum tolerated dose expected in 2H 2027.Dosing completed for first 4 dose levels Determine maximum tolerated dose level in 2H 2027 Filing
  2. Sep 30, 2026
    n/a Fulgent completed an End of Phase 2 meeting with FDA in 3Q 2026 for FID-007 in R/M HNSCC.End of Ph2 meeting with FDA in 3Q 2026 Filing
  3. Jun 30, 2026
    positive FID-007 combined with cetuximab demonstrated an objective response rate of 61.9% and median progression-free survival of 6.7 months in R/M HNSCC as of June 2026.In an ongoing Phase 2, open-label trial and as of June 2026, FID-007 demonstratedencouraging clinical activity when combined with cetuximab in patients with R/M HNSCC. Filing

For subscribers

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