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Spots Global Cancer Trial Database for Advanced Lung Cancer Treatment With Metformin and Chemo-Radiotherapy

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Advanced Lung Cancer Treatment With Metformin and Chemo-Radiotherapy

Official Title: A Phase II Study to Investigate a Combination of Metformin With Chemo-Radiotherapy in Patients With Locally Advanced Non-Small Cell Lung Cancer

Study ID: NCT02115464

Conditions

Lung Cancer

Study Description

Brief Summary: ALMERA is a randomized, phase II, open label study in patients with locally advanced non-small cell lung cancer (NSCLC) which will compare standard radiotherapy plus concurrent chemotherapy with or without consolidation versus the same treatment plus concurrent Metformin continuing for 12 months. Metformin is a well tolerated and inexpensive drug that has the potential to improve cancer patient outcomes.

Detailed Description: This is a randomized, phase II, open label study in patients with locally advanced NSCLC which will compare standard RT (60-63 Gy for 6 weeks) plus concurrent Cisplatin-based chemotherapy (CRT) with or without consolidation (standard arm) vs the same CRT with or without consolidation plus treatment with Metformin concurrent with CRT and continuing for a total of 12 months (experimental arm). Ninety-four eligible and consenting patients will be randomized to one of the two treatment arms. Patients randomized to the experimental arm will receive Metformin (2000 mg/day) for a period of 12 months. Patients will be continuously evaluated for toxicity, will be assessed weekly at clinic visits during concurrent CRT treatment with or without consolidation and at follow up clinic visits at 3, 6, 9 and 12 months (from the date of randomization). Disease progression will be evaluated every 3 months for up to 12 months. All patients will be followed for up to 24 months (2 years) for survival. The primary objective of this study is to determine the effect of Metformin on the proportion of patients free of disease progression at 12 months after initiation of drug treatment.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Cross Cancer Institute, Edmonton, Alberta, Canada

CancerCare Manitoba, Winnipeg, Manitoba, Canada

Juravinski Cancer Centre, Hamilton, Ontario, Canada

Cancer Centre of Southeastern Ontario at Kingston General Hospital, Kingston, Ontario, Canada

Grand River Regional Cancer Centre, Kitchener, Ontario, Canada

Walker Family Cancer Centre - Niagara Health System, St. Catharines, Ontario, Canada

Montreal General Hospital - McGill, Montreal, Quebec, Canada

Contact Details

Name: Theodoros Tsakiridis, MD

Affiliation: Juravinski Cancer Centre, Hamilton, Ontario, Canada

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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