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Clinical Trials in China / NCT06500234
Recruiting Phase 3

Nutrition Impact on Immunotherapy of Cancer

NCT06500234 · tracked via the Priya Life Science China tracker
Sponsor
Qingdao Central Hospital
Phase
Phase 3
Started
2024-06-01
Last updated
2024-07-15

Condition(s) studied

Nutrition DisordersImmunotherapyCancerSurvival, Prosthesis

Investigational drug(s) / intervention(s)

Megestrol Acetate and olanzapineStarch powder 50 mg

Megestrol Acetate and olanzapine: megestrol acetate, 160 mg, oral everyday; olanzapine 2.5 mg, oral everyday

Starch powder 50 mg: Starch powder 50 mg, oral, everyday

Study summary

This study investigates nutritional status and outcomes of immuntherapy in cancer patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of cancer, malnutrition Age \>18 years Performance status ECOG of 0 or 2. Life expectancy ≥ 6 months. At least one lesion measurable as defined by standard imaging criteria for the patient's tumor type (RECIST v1.1) Patients must have normal organ and bone marrow function measured within 28 days prior to administration of study treatment Postmenopausal or evidence of non-childbearing status for women of childbearing potential Patient is willing and able to comply with the protocol for the duration of the study. For all oral medications patients must be able to comfortably swallow capsules; Exclusion Criteria: * Patients unable to swallow orally administered medication and patients with Impairment of gastrointestinal (GI) function or GI disease that may significantly alter drug absorption of oral drugs History of allogenic organ, bone marrow or double umbilical cord blood transplantation. Active or prior documented autoimmune or inflammatory disorders Uncontrolled intercurrent illness or patient considered a poor medical risk due to a serious, uncontrolled medical disorder, including but not limited to, ongoing or active infection, symptomatic congestive heart failure Currently taking medications with known risk of prolonging the QT interval or inducing Torsades de Pointes.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Qingdao Central Hospital Qingdao Shandong Recruiting

More Qingdao Central Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06500234 on ClinicalTrials.gov ↗ ← All trials in China