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Spots Global Cancer Trial Database for A Study of Xeloda (Capecitabine) as Adjuvant Monotherapy in Patients With Colon Cancer.

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Trial Identification

Brief Title: A Study of Xeloda (Capecitabine) as Adjuvant Monotherapy in Patients With Colon Cancer.

Official Title: An Open Label Study to Evaluate the Safety of Xeloda as Adjuvant Monotherapy in Patients Who Have Undergone Surgery for Colon Cancer, Dukes Stage C.

Study ID: NCT00502671

Study Description

Brief Summary: This single arm study will evaluate the safety profile of Xeloda as monotherapy for adjuvant treatment of colon cancer. All patients will receive Xeloda 1250mg/m2 p.o. twice daily as intermittent treatment (3 week cycles consisting of 2 weeks of treatment followed by 1 week without treatment). The anticipated time on study treatment is 3-12 months, and the target sample size is 500+ individuals.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

, Arkhangelsk, , Russian Federation

, Astrakhan, , Russian Federation

, Barnaul, , Russian Federation

, Belgorod, , Russian Federation

, Chelyabinsk, , Russian Federation

, Ekaterinburg, , Russian Federation

, Irkutsk, , Russian Federation

, Izhevsk, , Russian Federation

, Kaluga, , Russian Federation

, Kazan, , Russian Federation

, Kazan, , Russian Federation

, Kirov, , Russian Federation

, Kostroma, , Russian Federation

, Krasnodar, , Russian Federation

, Kursk, , Russian Federation

, Lipetsk, , Russian Federation

, Moscow, , Russian Federation

, Moscow, , Russian Federation

, Moscow, , Russian Federation

, Moscow, , Russian Federation

, Moscow, , Russian Federation

, Moscow, , Russian Federation

, Nizhny Novgorod, , Russian Federation

, Novgorod Veliky, , Russian Federation

, Obninsk, , Russian Federation

, Orenburg, , Russian Federation

, Perm, , Russian Federation

, Rostov-na-donu, , Russian Federation

, Ryazan, , Russian Federation

, Salekhard, , Russian Federation

, Samara, , Russian Federation

, Smolensk, , Russian Federation

, Soshi, , Russian Federation

, St Petersburg, , Russian Federation

, St Petersburg, , Russian Federation

, Stavropol, , Russian Federation

, Surgut, , Russian Federation

, Tollyatti, , Russian Federation

, Tomsk, , Russian Federation

, Tomsk, , Russian Federation

, Tumen, , Russian Federation

, Tver, , Russian Federation

, UFA, , Russian Federation

, UFA, , Russian Federation

, Volgograd, , Russian Federation

, Yuzhno-Sakhalinsk, , Russian Federation

Contact Details

Name: Clinical Trials

Affiliation: Hoffmann-La Roche

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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