Real-World Study on Nano-Crystalline Megestrol Acetate for Cachexia in TKI-Treated Advanced Digestive Tumors

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChangchun GeneScience Pharmaceutical Co., Ltd.

About this trial

This study is a prospective, observational clinical study aimed at evaluating the efficacy of Megestrol Acetate for cachexia in patients with advanced digestive system tumors receiving TKI-based therapy.

Eligibility criteria

Qualifiers

Voluntarily sign a written informed consent (ICF).

Age ≥ 18 years at enrollment.

Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.

Life expectancy ≥ 3 months.

Disqualifiers

Gastrointestinal obstruction.

Anorexia due to difficulty in eating caused by neurosis, mental illness, or pain.

Comorbidities such as severe cerebrovascular, cardiac, renal, or liver diseases.

Major surgery or trauma within the last month.

Trial design

Treatments tested in this trial

  • Nano-crystalline Megestrol Acetate Oral Suspension
  • TKI-Based Therapy

Treatment groups

120 Participants
are divided into 2 treatment groups