Who are FUDR +oxaliplatin's main competitors?

No direct comparators detected in our index.

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Every 30 minutes from primary sources (FDA, EMA, MHRA, PMDA, ClinicalTrials.gov, USPTO). Subscribe to the RSS feed below for push alerts.

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Last reviewed 2026-06-10 · How we verify

FUDR +oxaliplatin — Competitive Intelligence Brief

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

FUDR +oxaliplatin (FUDR +oxaliplatin) competitive landscape: 0 comparators, recent regulatory actions, upcoming PDUFA, patent timeline. Class: Chemotherapy combination (fluoropyrimidine + platinum agent). Area: Oncology.

phase 3 Chemotherapy combination (fluoropyrimidine + platinum agent) Thymidylate synthase (FUDR); DNA (oxaliplatin cross-linking) Oncology Small molecule Live · refreshed every 30 min

Target snapshot

FUDR +oxaliplatin (FUDR +oxaliplatin) — Xu jianmin. FUDR (floxuridine) and oxaliplatin work together as a chemotherapy combination to inhibit DNA synthesis and cross-link DNA, killing rapidly dividing cancer cells.

Comparator set

Auto-detected by same drug class / molecular target / therapeutic area, ranked by phase + recency. Override with ?vs=slug1,slug2,….

Drug	Generic	Sponsor	Phase	Class	Target	Approval / PDUFA
FUDR +oxaliplatin TARGET	FUDR +oxaliplatin	Xu jianmin	phase 3	Chemotherapy combination (fluoropyrimidine + platinum agent)	Thymidylate synthase (FUDR); DNA (oxaliplatin cross-linking)

Recent regulatory actions (last 90 days)

No regulatory actions in the last 90 days for this set.

Upcoming PDUFA dates (next 180 days)

No PDUFA dates in the next 180 days for this set.

Patent timeline (forward window)

No upcoming patent expiries for this set.

Sponsor landscape (Chemotherapy combination (fluoropyrimidine + platinum agent) class)

Xu jianmin · 1 drug in this class

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Cite this brief

Drug Landscape (2026). FUDR +oxaliplatin — Competitive Intelligence Brief. https://druglandscape.com/ci/fudr-oxaliplatin. Accessed 2026-06-10.

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing