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capecitabine

Generic: CAPECITABINE·Brand: CAPECITABINE, XELODA, Xeloda

capecitabine: 107 clinical trials tracked.

capecitabine evidence translation

What we can confirm

107 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about capecitabine, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 28 study sponsors
Clinical Trials (107)showing 10 most recent

A Multicenter, Open-label, Treatment Protocol of Tucatinib in Combination With Capecitabine and Trastuzumab in Patients With Previously Treated Unresectable Locally Advanced or Metastatic HER2+ Breast Carcinoma

Approved for marketing
Expanded AccessSeagen, a wholly owned subsidiary of Pfizer

A Biomarker Enrichment Trial of Anti-EGFR Agents in Patients With Advanced Colorectal Cancer (aCRC) With Wild-type RAS and Right Primary Tumour Location (Right-PTL).

NCT07094893·Phase 4
Not yet recruiting

Primary endpoint: Early tumour shrinkage (ETS)

InterventionalRandomizedopen280 targetStarted 2026-09Completion 2030-03Gruppo Oncologico del Nord-Ovest

Combining Capecitabine/Oxaliplatin Chemotherapy With Cemiplimab Alone or in Combination With Fianlimab or REGN7075 for the Neoadjuvant Treatment of Locally Advanced Rectal Cancer

NCT07281768·Phase 2
Recruiting

Primary endpoint: Pathologic complete response (pCR) rate

InterventionalRandomizedopen66 targetStarted 2026-07Completion 2030-071 site · United StatesSidney Kimmel Comprehensive Cancer Center at Johns Hopkins

A Phase II Study Evaluating the Efficacy and Safety of SKB315 Combination Therapy in Claudin18.2 Positive Patients With Unresectable Locally Advanced or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

NCT07609667·Phase 2
Not yet recruiting

Primary endpoint: Objective Response Rate (ORR)

InterventionalRandomizedopen80 targetStarted 2026-06Completion 2029-061 site · ChinaSichuan Kelun-Biotech Biopharmaceutical Co., Ltd.

An Open-Label, Single-Arm, Phase 2 Study to Evaluate the Efficacy and Safety of Tislelizumab Plus Chemotherapy in a First-Line Setting for Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Adenocarcinoma and Esophageal Squamous Cell Carcinoma in US Racial and Ethnic Minority Patients

NCT07554521·Phase 2·ONC
Recruiting

Primary endpoint: Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)

Interventionalopen30 targetStarted 2026-04Completion 2031-128 sites · United StatesBeOne Medicines

A Two-part, Seamless, Multicenter, Randomized, Open-label, Adaptive Phase II/III Study of the Blood-brain Barrier Penetrant RO7771950 Versus Tucatinib, Both in Combination With Trastuzumab and Capecitabine, in Patients With Pretreated Unresectable Locally Advanced or Metastatic HER2-Postivie Breast Cancer, With or Without Central Nervous System Metastases

NCT07413939·Phase 2·ENTA
Not yet recruiting

Primary endpoint: Progression-free Survival (PFS) as Determined by Blinded Independent Central Review (BICR)

InterventionalRandomizedopen650 targetStarted 2026-04Completion 2032-08Hoffmann-La Roche

A Randomized, Open-Label, Multicenter Phase III Study of Tecotabart Vedotin Plus Tislelizumab Versus Tislelizumab Plus Chemotherapy as First-Line Treatment in Patients With CLDN18.2-Positive, Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

NCT07385703·Phase 3
Recruiting

Primary endpoint: Progression-free survival (PFS)

InterventionalRandomizedopen752 targetStarted 2026-04Completion 2030-0550 sites · ChinaShanghai Chia Tai Tianqing Pharmaceutical Technology Development Co., Ltd.

An Open-label, Multicenter, Phase II Clinical Study to Evaluate the Efficacy and Safety of LBL-024 in Combination With Other Drugs for the Treatment of Patients With Advanced Solid Tumour[Substudy Number 04]

NCT07390383·Phase 2
Recruiting

Primary endpoint: Objective Response Rate (ORR)

InterventionalRandomizedopen110 targetStarted 2026-04Completion 2028-057 sites · ChinaNanjing Leads Biolabs Co.,Ltd

A Multicenter, Phase III, Randomized Controlled Clinical Trial of Sintilimab Versus Mitomycin in Combination With Capecitabine and Intensity-Modulated Radiotherapy in the Treatment of Limited-stage Anal Squamous Cell Carcinoma

NCT07692152·Phase 3
Recruiting

Primary endpoint: Clinical Complete Response (cCR) Rate

InterventionalRandomizedopen350 targetStarted 2026-03Completion 2029-032 sites · ChinaCancer Institute and Hospital, Chinese Academy of Medical Sciences

A Randomized, Open-label, Controlled, Multicenter Phase 3 Clinical Trial of AK104 for Neoadjuvant/Adjuvant Treatment of Microsatellite Instability-high or Mismatch Repair-deficient, Resectable Colon Cancer

NCT07412613·Phase 3·MRUS
Not yet recruiting

Primary endpoint: Pathologic Complete Response (pCR) rate as assessed by investigator

InterventionalRandomizedopen386 targetStarted 2026-03Completion 2031-031 site · ChinaAkeso