An Exploratory Clinical Study to Evaluate the Safety, Tolerability, Immune Response and Preliminary Efficacy of LM103 Injection in Combination With PD-1 in Patients With Advanced Solid Tumours

Suzhou BlueHorse Therapeutics Co., Ltd.1 site in 1 country10 target enrollmentJanuary 23, 2024

ConditionsSolid Cancer

InterventionsLM103

DrugsLM103

Overview

Phase: Early Phase 1
Intervention: LM103
Conditions: Solid Cancer
Sponsor: Suzhou BlueHorse Therapeutics Co., Ltd.
Enrollment: 10
Locations: 1
Primary Endpoint: Adverse events (AE), Serious adverse event (SAE) and immune related adverse events (irAE)
Status: Recruiting
Last Updated: last year

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

This is an exploratory clinical study evaluating the safety, tolerability, immune response and preliminary efficacy of LM103 Injection in combination with PD-1 in patients with advanced solid tumours. The research treatment includes LM103 injection, IL-2 therapy, PD-1 therapy,fludarabine and cyclophosphamide.

Registry

clinicaltrials.gov

Start Date

January 23, 2024

End Date

June 2027

Last Updated

last year

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Suzhou BlueHorse Therapeutics Co., Ltd.

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•The expected survival time is not less than 3 months.
•Clinical performance status of Eastern Cooperative Oncology Group (ECOG) 0-
•Patients with advanced solid tumors confirmed by histology or cytology: advanced Melanoma, cervical cancer/ovarian cancer, head and neck squamous cell cancer, non-small cell lung cancer, esophageal cancer and other solid tumors that have failed standard treatment regimens, cannot tolerate standard treatment, refuse or do not have standard treatment regimens available.
•The patient has lesions that can be used for surgical resection (\>1.5 cm3) or biopsy puncture (no less than 6 lesions) for LM103 manufacturing.
•At least one measurable lesion as the target lesion after collecting tumor tissue from the patient (RECIST v1.1 criteria).
•Laboratory tests results during the screening period indicate that the subjects have sufficient organ function.

Exclusion Criteria

•Have a medical history of other malignant tumors other than the disease under study in the past 5 years, except for malignant tumors that can be expected to recover after treatment (including but not limited to thyroid cancer, cervical Carcinoma in situ, basal or squamous cell skin cancer or Ductal carcinoma in situ of the breast treated by radical surgery).
•LM103 received systematic therapy of antineoplastic drugs (including chemotherapy, small molecule targeted drug therapy, Hormone replacement therapy, etc.), or local antineoplastic therapy (such as radiotherapy, palliative radiotherapy for bone metastases\>2 weeks before the start of the study and intracranial stereotactic radiotherapy or resection of a single brain metastasis\>3 weeks before the start of the study were acceptable) within 4 weeks before LM103 infusion; Or received clinical investigational drugs or equipment treatment.
•Adverse reactions caused by previous treatment have not recovered to CTCAE (version 5.0) level 1 or below (excluding hair loss and neurotoxicity, which have been determined by the researchers to be irreparable and level 2 hypothyroidism for a long time).
•Previously received allogeneic hematopoietic stem cell transplantation or solid organ transplantation.

Arms & Interventions

Participant Group

Treatment includes LM103 injection and PD-1

Intervention: LM103

Outcomes

Primary Outcomes

Adverse events (AE), Serious adverse event (SAE) and immune related adverse events (irAE)

Time Frame: through study completion, an average of 1 year estimate

Incidence and severity of AE, SAE and irAE; Abnormal changes in laboratory and other tests with clinical significance.

Secondary Outcomes

Objective response rate (ORR)(through study completion, an average of 1 year estimate)
Duration of response (DOR)(through study completion, an average of 1 year estimate)
Disease control rate (DCR)(through study completion, an average of 1 year estimate)
Time to response (TTR)(through study completion, an average of 1 year estimate)
Time to disease progression (TTP)(through study completion, an average of 1 year estimate)
Progression free survival (PFS)(through study completion, an average of 1 year estimate)
Overall survival (OS)(through study completion, an average of 1 year estimate)