EUCTR2007-004521-22-IT
Active, not recruiting
Not Applicable
Phase II, Randomised, double-blind, two-arm, parallel study of Vandetanib (ZACTIMA , ZD6474) plus Gemcitabine (Gemzar ) or Gemcitabine plus Placebo as first line treatment of advanced (stage IIIB or IV) Non Small Cell Lung Cancer (NSCLC) Elderly patients - Zelig
DrugsGEMZAR
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- ASTRAZENECA
- Status
- Active, not recruiting
- Last Updated
- 13 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Provision of informed consent
- •2\.Female or male aged 70 years or above
- •3\.Histologic or cytologic confirmation of advanced NSCLC (stage IIIB with supraclavicular lymph node metastases or pleural effusion or stage IV) on entry into study
- •4\.No prior anti\-cancer therapies except in the adjuvant setting
- •5\.WHO Performance status 0 \- 2
- •6\.One or more measurable lesions at least 10 mm in the longest diameter (LD) by spiral CT scan or 20 mm with conventional techniques according to RECIST criteria
- •7\.Life expectancy of 12 weeks or longer
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) no
Exclusion Criteria
- •1\.Mixed small cell and non\-small cell lung cancer histology
- •2\.Patients have received prior anti\-cancer therapy except in the adjuvant setting
- •3\.Prior treatment with gemcitabine
- •4\.Prior treatment with VEGFR TKIs (previous treatment with bevacizumab \[Avastin] in the adjuvant setting is permitted)
- •5\.Brain metastases or spinal cord compression, unless treated at least 4 weeks before entry, and stable without steroid treatment for 10 days
- •6\.The last radiation therapy within 4 weeks before the start of study therapy, not including local palliative radiation
- •7\.The last dose of prior chemotherapy or other anti\-cancer therapy is discontinued less than 3 weeks before the start of study therapy (6 weeks for nitrosoureas, mitomycin, and suramin)
- •8\.Major surgery within 4 weeks before entry, or incompletely healed surgical incision
- •Others are specificied in the protocol
Outcomes
Primary Outcomes
Not specified
Similar Trials
Recruiting
Phase 2
evaluate efficacy and safety of SpikoGen® vaccine on healthy adults to prevent COVID-19 diseaseCOVID-19.COVID-19, virus identifiedU07.1IRCT20150303021315N23CinnaGen Company400
Active, not recruiting
Not Applicable
A study to investigate the analgesic efficacy of AZD2423 compared with placebo after 28 days treatment in patients with posttraumatic neuralgiaPosttraumatic Neuralgia (neuropathic pain)MedDRA version: 14.1Level: LLTClassification code 10054095Term: Neuropathic painSystem Organ Class: 10029205 - Nervous system disordersTherapeutic area: Diseases [C] - Nervous System Diseases [C10]EUCTR2010-019785-90-SEAstraZeneca AB135
Active, not recruiting
Phase 1
A Phase IIa, Double-blind, Randomised, Parallel-group, Multi-centre Study to Evaluate the Analgesic Efficacy of 28 Days Oral Administration of AZD2423 Compared to Placebo in Patients with Posttraumatic NeuralgiaPosttraumatic Neuralgia (neuropathic pain)MedDRA version: 12.1Level: LLTClassification code 10054095Term: Neuropathic painEUCTR2010-019785-90-FRAstraZeneca AB135
Active, not recruiting
Not Applicable
A study to investigate the analgesic efficacy of AZD2423 compared with placebo after 28 days treatment in patients with posttraumatic neuralgiaPosttraumatic Neuralgia (neuropathic pain)MedDRA version: 14.0Level: LLTClassification code 10054095Term: Neuropathic painSystem Organ Class: 10029205 - Nervous system disordersTherapeutic area: Diseases [C] - Nervous System Diseases [C10]EUCTR2010-019785-90-GBAstraZeneca AB135
Active, not recruiting
Not Applicable
A study to investigate the analgesic efficacy of AZD2423 compared with placebo after 28 days treatment in patients with posttraumatic neuralgiaEUCTR2010-019785-90-DKAstraZeneca AB135