Gefitinib, 5-fluorouracil, leucovorin and radiotherapy

Phase 1/2Terminated
0 views this week 0 watching💤 Quiet
Interest: 24/100
24
Hype Score

Development Stage

Pre-clinical
2
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Subjects With Resectable Local or Locally Advanced, Non-Metastatic (T2-T4, N0-N3, M0; Stages II and III) and Histologically-Confirmed Intestinal GC

Conditions

Subjects With Resectable Local or Locally Advanced, Non-Metastatic (T2-T4, N0-N3, M0; Stages II and III) and Histologically-Confirmed Intestinal GC

Trial Timeline

Jul 1, 2003 → Feb 1, 2004

About Gefitinib, 5-fluorouracil, leucovorin and radiotherapy

Gefitinib, 5-fluorouracil, leucovorin and radiotherapy is a phase 1/2 stage product being developed by AstraZeneca for Subjects With Resectable Local or Locally Advanced, Non-Metastatic (T2-T4, N0-N3, M0; Stages II and III) and Histologically-Confirmed Intestinal GC. The current trial status is terminated. This product is registered under clinical trial identifier NCT00237900. Target conditions include Subjects With Resectable Local or Locally Advanced, Non-Metastatic (T2-T4, N0-N3, M0; Stages II and III) and Histologically-Confirmed Intestinal GC.

What happened to similar drugs?

6 of 16 similar drugs in Subjects With Resectable Local or Locally Advanced, Non-Metastatic (T2-T4, N0-N3, M0; Stages II and III) and Histologically-Confirmed Intestinal GC were approved

Approved (6) Terminated (1) Active (10)

Hype Score Breakdown

Clinical
9
Activity
0
Company
15
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT00237900Phase 1/2Terminated

Competing Products

20 competing products in Subjects With Resectable Local or Locally Advanced, Non-Metastatic (T2-T4, N0-N3, M0; Stages II and III) and Histologically-Confirmed Intestinal GC

See all competitors
ProductCompanyStageHype Score
ENZ215 + EU Sourced Prolia + US Sourced ProliaAlkem LaboratoriesPhase 1
29
Moxifloxacin + Placebo + Lanifibranor + PlaceboInventivaPhase 1
23
PegilodecakinEli LillyPhase 1
29
CT-P41 + EU-approved ProliaCelltrionPhase 1
29
CT-P55 + US-licensed Cosentyx + EU-approved CosentyxCelltrionPhase 1
29
CT-P52CelltrionPhase 1
36
CT-P47 + EU-approved RoActemra,CelltrionPhase 1
25
CT-P47 + CT-P47CelltrionPhase 1
25
CT-P43 + EU-approved Stelara + US-licensed StelaraCelltrionPhase 1
29
CT-P43 + CT-P43CelltrionPhase 1
29
YHP2406 + YHR2501YuhanPhase 1
29
YH35324 + Placebo + OmalizumabYuhanPhase 1
29
YHP2511 + YHP2511AYuhanPhase 1
36
YH35324 + Placebo + OmalizumabYuhanPhase 1
29
Bempedoic acid + Ezetimibe + AtorvastatinDaiichi SankyoPhase 1
29
Quizartinib dihydrochloride + 14C-Quizartinib solution for infusionDaiichi SankyoPhase 1
29
Bempedoic acid + Ezetimibe + RosuvastatinDaiichi SankyoPhase 1
29
Quizartinib + RufinamideDaiichi SankyoPhase 1
29
QuizartinibDaiichi SankyoPhase 1
29
Efavirenz + QuizartinibDaiichi SankyoPhase 1
29