HV-101 for Patients With Advanced Solid Tumors

Phase 1

Recruiting

• Conditions: Advanced Solid Tumors
• Interventions: Biological: HV-101

• Registration Number: NCT05868915
• Lead Sponsor: Hervor Therapeutics

Brief Summary

Background:

Tumor-infiltrating lymphocyte (TIL) therapy is a type of adoptive cellular therapy by harvesting infiltrated lymphocytes from tumors, culturing and amplifying them in vitro and then infusing back to treat patients. TIL therapy has shown strong efficacy for the treatment of solid tumors, and has achieved high objective response rates in multiple cancers.

Objective:

To evaluate the safety and efficacy of HV-101 for the treatment of advanced solid tumors.

Eligibility:

Adults aging 18-75 with advanced solid tumors

Design:

1. Patients will undergo screening tests, including imaging procedures, heart and lung tests, and lab tests.

2. Freshly resected patient tumors were dissected by the surgeon.

3. TIL cells were isolated from the patient's tumor tissue in the laboratory, then cultured in vitro, activated and expanded.

4. HV-101 will be re-infused into the patient.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-05-11
• Study First Submitted QC: 2023-05-11
• Study First Posted: 2023-05-22
• Study Start: 2023-08-04
• Status Verified: 2024-03
• Last Update Submitted: 2024-03-01
• Last Update Posted: 2024-03-04
• Primary Completion: 2025-05-31
• Study Completion: 2026-03-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

1. Be able to understand and sign the Informed of Consent Document. Be willing to follow the procedure and protocol of the clinical trial.

2. Age ≥ 18 years and ≤ 75 years.

3. Expected survival time > 3 months.

4. ECOG score 0-1.

5. At least one lesion that could undergo surgery or biopsy to obtain tumor tissue for TIL preparation

6. At least 1 measurable lesion (according to RECIST v1.1).

7. Metastatic or recurrent solid tumors confirmed by histopathology. Refractory to standard treatment evaluated by radiological assessment.

8. Hematology should at least meet the following criteria:

   • Absolute neutrophil count (ANC) ≥ 1.5× 109/L；
   • Platelet (PLT） ≥ 75× 109/L；
   • Hemoglobin (HGB) ≥ 90 g/L.

9. Liver and kidney function are normal:

   • Serum creatinine (Cr) ≤ 1.5 times of upper limit of normal (ULN) or creatine clearance ≥ 60 ml/min;
   • Serum Alanine aminotransferase (ALT) or/and Aspartate aminotransferase (AST) ≤ 2.5 times of ULN;
   • Total bilirubin (TBIL) ≤ 1.5 times of ULN.

10. Blood coagulation function is normal:

    • Prothrombin time (PT) ≤ 1.5 ULN;
    • International Normalized Ratio (INR) ≤ 1.5 ULN;
    • or Activated Partial Thromboplastin Time (APTT) ≤ 1.5 ULN.

11. Women of childbearing potential should be ascetic or take contraception since the signing of ICF to 24 weeks or later after the last administration of drug.

Exclusion Criteria

1. Under pregnancy or lactation, or positive based on blood pregnancy test.
2. Severe allergic to related ingredients in the clinical trial.
3. Received any other investigational treatment within 28 days before the administration of HV-101.
4. History of other known malignant tumors within the previous 5 years.
5. Primary central nerve system (CNS) cancer, or Participants with CNS metastasis after localized treatment.
6. Participants with any active autoimmune disease, a history of autoimmune disease, or a history or syndrome requiring treatment with systemic steroids or immunosuppressive drugs.
7. Immunodeficiency including HIV positive, acquired or primary immunodeficiency.
8. Participants with ≥ grade 3 thromboembolic events within 6 months or under thrombolysis treatment.
9. Participants with hereditary or acquired hemorrhagic disease.
10. Participants with clinical cardiovascular disease or symptoms
11. Participants with active infection.
12. Participants with active pulmonary tuberculosis infection.
13. Participants with positive hepatitis B surface antigen or positive hepatitis B core antibody or positive hepatitis C virus antibody.
14. Treponema pallidum antibody positive.
15. Participants received major surgery or under severe injury within 28 days before HV-101 infusion.
16. Participants who received live vaccine or attenuated live vaccine 28 days before HV-101 infusion.
17. Participants who have drug addiction history, alcoholism, or drug users.
18. Participants who received cell therapy before enrollment.
19. Participants who have contraindications to the treatment of IL-2 injection.
20. Participants not suitable for the clinical trial evaluated by the investigators.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
HV-101	HV-101	Participants with Advanced Solid Tumors Interventions: Biological: HV-101 Drug: IL-2 Drug: Fludarabine Drug: Cyclophosphamide

Primary Outcome Measures

Name	Time	Method
Safety of HV-101	Day 0 - Day 730	The safety of HV-101 will be assessed based on the totality of dose-limiting toxicity (DLT) and adverse event (AE) data collected during this phase.

Secondary Outcome Measures

Name	Time	Method
Overall survival (OS)	Day 0 - Day 730	To evaluate the time from the date of HV-101 infusion to death due to any cause.
Overall Response Rate (ORR)	Day 0 - Day 730	To evaluate the proportion of participants who have a confirmed partial response (PR) and complete response (CR) per RECIST v1.1 as assessed by the investigator.
Duration of Response (DOR)	Day 0 - Day 730	To evaluate the duration from the time that criteria are met for CR or PR per RECIST v1.1 as assessed by the investigator until disease progression or death due to any cause.
Progression free survival (PFS)	Day 0 - Day 730	To evaluate the time from the date of HV-101 infusion until disease progression per RECIST v1.1 as assessed by the investigator or death due to any cause.
Disease Control Rate (DCR)	Day 0 - Day 730	To evaluate the percentage of participants with a best overall confirmed response of CR or PR at any time plus stable disease (SD) per RECIST v1.1 as assessed by the investigator.

Trial Locations

Locations (1)

Renmin Hospital of Wuhan University; 🇨🇳 Wuhan, Hubei, China