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NCT00265876
AZD0530 and Gemcitabine in Locally Advanced/Metastatic Pancreatic Cancer That Cannot Be Removed By Surgery
Phase 1, PHASE2 trial testing AZD0530 in Pancreatic Cancer in 34 participants. Completed in 6 January 2012.
8 January 2009
Quick facts
| Lead sponsor | NCIC Clinical Trials Group |
|---|---|
| Phase | Phase 1, PHASE2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 34 |
| Start date | 26 April 2006 |
| Primary completion | 8 January 2009 |
| Estimated completion | 6 January 2012 |
| Sites | 4 locations across Canada |
Drugs / interventions tested
- AZD0530 — full drug profile →
- gemcitabine hydrochloride — full drug profile →
Conditions studied
- Pancreatic Cancer — all drugs for Pancreatic Cancer →
Sponsor
NCIC Clinical Trials Group
Who can join
Adults 18 to 120, any sex, with Pancreatic Cancer. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
RATIONALE: AZD0530 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving AZD0530 together with gemcitabine may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of AZD0530 when given together with gemcitabine and to see how well they work in treating patients with locally advanced or metastatic pancreatic cancer that cannot be removed by surgery.
Publications & conference data
6 peer-reviewed publications reference this trial (live from Europe PMC):
-
SRC: a century of science brought to the clinic.
Aleshin A, Finn RS. · · 2010 · cited 170× · PMID 20689754 · DOI 10.1593/neo.10328 -
Resistance to Gemcitabine in Pancreatic Ductal Adenocarcinoma: A Physiopathologic and Pharmacologic Review.
Koltai T, Reshkin SJ, Carvalho TMA, Di Molfetta D, et al · · 2022 · cited 77× · PMID 35626089 · DOI 10.3390/cancers14102486 -
Targeting epidermal growth factor receptor and SRC pathways in head and neck cancer.
Egloff AM, Grandis JR. · · 2008 · cited 65× · PMID 18544443 · DOI 10.1053/j.seminoncol.2008.03.008 -
Targeting the complexity of Src signalling in the tumour microenvironment of pancreatic cancer: from mechanism to therapy.
Parkin A, Man J, Timpson P, Pajic M. · · 2019 · cited 40× · PMID 31330086 · DOI 10.1111/febs.15011 -
Functional roles of SRC signaling in pancreatic cancer: Recent insights provide novel therapeutic opportunities.
Poh AR, Ernst M. · · 2023 · cited 34× · PMID 37120696 · DOI 10.1038/s41388-023-02701-x -
Dual Drug Repurposing: The Example of Saracatinib.
Ramos R, Vale N. · · 2024 · cited 17× · PMID 38674150 · DOI 10.3390/ijms25084565
Verify or expand the search:
- PubMed search for NCT00265876
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other NCIC Clinical Trials Group trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00265876 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by NCIC Clinical Trials Group
- Last refreshed: 4 August 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00265876.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing