Recent Updates
Recently added Catalysts

Erlotinib orally days 1-28

Phase 1

Pancreatic Cancer | Small molecule | Oncology |Roche Holding AG|Trials Updated: Oct 14, 2016

Erlotinib orally days 1-28 target and mechanism

Molecular targetEGFR
Target classInhibitor
ModalitySmall molecule
ChEMBLCHEMBL553

Success Probability

Subscribe to view

Market & Valuation

Subscribe to view

Trial Design

UNCONTROLLEDDMC
Total Trials1
Total Enrollment44

FDA Designations

No designations recorded

Erlotinib orally days 1-28 clinical trials

Erlotinib orally days 1-28 · 1 trial · 1 indication

Phase 1 1
NCT00260364Combining Erlotinib Plus Bevacizumab and Gemcitabine Plus Capecitabine to Treat Advanced Pancreatic CancerPancreatic Cancer
COMPLETED44 Analytics
PHASE1COMPLETED
Combining Erlotinib Plus Bevacizumab and Gemcitabine Plus Capecitabine to Treat Advanced Pancreatic Cancer
Pancreatic CancerUnlock trial analytics

Study Endpoints

Primary Endpoints

Part A (Phase I): Dose-limiting Toxicity (DLT)
Part B (Phase II): Overall response rate (complete response and partial response)

Secondary Endpoints

The secondary efficacy objectives of the trial are: One year survival and median overall survival
Progression free survival, Disease control rate.
The secondary safety objectives are: Toxicity,Quality of life
Unlock Study Endpoints

Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Interventions

NameTypeDescription
Gemcitabine 1000 mg/m2 iv days 1, 8, 15 of a 28 day cycleDRUG -
Capecitabine orally days 1 -21DRUG -
Erlotinib 100 mg orally days 1-28DRUG -
Bevacizumab 5 mg/kg intravenously every 2 weeksDRUG -
Unlock Study Design Details

Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites1

DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed adenocarcinoma of the pancreas * Locally advanced or metastatic disease * Not amenable to curative resection * No invasion of adjacent organs (e.g., duodenum or stomach) by CT scan * Unidimensionally measurable disease as assessed...

Countries:United Kingdom
Unlock Eligibility Criteria

Competitive Landscape -Pancreatic Cancer 248 trials

Unlock Competitive Intelligence

Frequently asked questions about Erlotinib orally days 1-28

What is Erlotinib orally days 1-28?

Erlotinib orally days 1-28 is an oral dosing schedule of erlotinib, a small molecule EGFR inhibitor, given once daily on days 1 through 28 of a treatment cycle. It is being studied in pancreatic cancer. The regimen is also referred to as Erlotinib 100 mg orally days 1-28.

What is Erlotinib orally days 1-28 used for in pancreatic cancer?

Erlotinib orally days 1-28 is used in pancreatic cancer as part of a combination regimen. In the Phase 1 trial NCT00260364, it was given with bevacizumab plus gemcitabine and capecitabine to treat advanced pancreatic cancer. The study enrolled 44 adults in the United Kingdom.

What does Erlotinib orally days 1-28 target?

Erlotinib orally days 1-28 targets EGFR, the epidermal growth factor receptor. It is an EGFR inhibitor, a small molecule that blocks EGFR signaling. This mechanism underlies its investigation in pancreatic cancer, where EGFR pathway activity is relevant to tumor growth.

Who makes Erlotinib orally days 1-28?

Erlotinib orally days 1-28 is developed by Roche Holding AG, which trades under the ticker RHHBY. Roche is the company associated with this oral erlotinib regimen and the Phase 1 pancreatic cancer study evaluating it.

What phase is Erlotinib orally days 1-28 in?

Erlotinib orally days 1-28 is in Phase 1 development. It is investigational and has not been approved for pancreatic cancer. The single Phase 1 trial, NCT00260364, has been completed, and no active trials are ongoing for this regimen.

What clinical trials is Erlotinib orally days 1-28 in?

Erlotinib orally days 1-28 was evaluated in one completed Phase 1 trial, NCT00260364, titled Combining Erlotinib Plus Bevacizumab and Gemcitabine Plus Capecitabine to Treat Advanced Pancreatic Cancer. The trial enrolled 44 participants in the United Kingdom and was uncontrolled, non-randomized, and not double-blind.