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Study identifier: NCT07231120 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy of SXRN Injection in Patients With Cancer Cachexia

Condition: Cachexia-Anorexia Syndrome · Solid Tumor Malignancies  ·  Sponsor: Jiangsu Nutai Biologics Co., Ltd

PhasePhase 1
Planned participants54
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is a clinical study evaluating the safety, tolerability, pharmacokinetics (PK), and preliminary efficacy of SXRN Injection in cancer patients with anorexia-cachexia. Phase Ia employs a single-arm, open-label, dose-escalation design. Phase Ib, an extension of the study, utilizes a design of combination therapy with standard anti-tumor therapy for cancers including but not limited to pancreatic cancer, non-small cell lung cancer (NSCLC), and colon cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Ning Li  ·  +86 1087788713  ·  lining@cicams.ac.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Cancer Hospital Chinese Academy of Medical SciencesBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07231120