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A Phase II multicenter trial of Gemcitabine in combination with R1415 (erlotinibhydrochloride) in patients with unresectable pancreatic cancer (locally advanced or metastatic)

A Phase II multicenter trial of Gemcitabine in combination with R1415 (erlotinibhydrochloride) in patients with unresectable pancreatic cancer (locally advanced or metastatic)

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080220332
Enrollment
Unknown
Registered
2006-12-14
Start date
2006-12-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic cancer

Interventions

investigational material(s) Generic name etc : erlotinibhydrochloride INN of investigational material : Therapeutic category code : 429 Other antitumor agents Dosage and Administration for Investigat

Sponsors

Chugai Pharmaceutical Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria - Histologically or cytologically confirmed diagnosis of adenocarcinoma or adenosquamous of the pancreas cancer which is unresectable (locally advanced or metastatic). - ECOG performance status (PS) of 0, 1 or 2. - Adequate organ functions Exclusion criteria - The patient is currently suffering from such pulmonary disorders as sudden pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, active radioactive pneumonia, or drug-related pneumonia, or he/she has a history of such disease. - Patients have thoracic radiotherapy. - Prior treatment with Gemcitabine - Patients who have had treatment with any investigational drug within 4 weeks prior to entry. - Patients who have history of serious hypersensitivity reactions with any medicine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Safety (feasibility), efficacy

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026