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Use of TEGAFUR + GIMERACIL + OTERACIL combination in the management of tumor

A Multicenter Retrospective Observational Study on Real-World Utilization of TEGAFUR + GIMERACIL + OTERACIL in Solid Tumors - TEGO-INDIA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/06/112597
Enrollment
1000
Registered
2026-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Nil: Nil

Sponsors

Torrent Pharmaceuticals Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults aged more than 18 years. 2. Histologically or cytologically confirmed solid tumors 3. Received S-1 monotherapy or combination therapy for at least one cycle during the study period 4. Availability of clinical documentation or retrospective Patient-Reported Outcomes (PRO) data for baseline and follow-up.

Exclusion criteria

Exclusion criteria: 1. Diagnosis of haematological malignancy 2. Participation in an interventional clinical trial involving S-1 during the study period 3. Incomplete or missing treatment data at baseline and follow-up. 4. Pregnancy/lactation during therapy.

Design outcomes

Primary

MeasureTime frame
1. Drug utilization trend of S1 therapy by Tumour type 2. Assessment of line of therapy, intent of treatment, dosing & frequency of S1 therapyTimepoint: Baseline

Secondary

MeasureTime frame
1. Median duration of S-1 treatment in real-world settings 2. Incidence and type of adverse events (AEs)Timepoint: Baseline

Countries

India

Contacts

Public ContactDr Rathish Nair

Torrent Pharmaceuticals Ltd.

RATHISHNAIR@TORRENTPHARMA.COM7069000560

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026