A Study of ES014 in Patients With Locally Advanced or Metastatic Solid Tumours

Elpiscience Biopharma

Status and phase: Active, not recruiting; Phase 1

Conditions: Solid Tumor; Locally Advanced Solid Tumor; Metastatic Solid Tumor

Treatments: Drug: ES014

Study type: Interventional

Funder types: Industry

Identifiers

NCT05717348

ES014-1002

Details and patient eligibility

About

The purpose of this first-in-human, open-label, multicenter, non-randomized study designed to determine the maximum tolerated dose (MTD)/maximum administered dose (MAD), optimal biological dose (OBD), and recommended phase 2 dose (RP2D) of ES014 by evaluating the safety, tolerability, PK, pharmacodynamics, and preliminary clinical activity of ES014 administered intravenously to subjects with advanced solid tumors.

Enrollment: 120 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 1. Unresectable locally advanced or metastatic solid tumour diagnosed by pathology or cytology and which meets the criteria of 1) disease progression has occurred despite receiving standard treatment and no other standard treatment is available; or 2) standard treatment has been proven to be ineffective, intolerant or considered unsuitable.

  2. Provide tumor tissue samples.

  3. At least one measurable lesion per RECIST v1.1.

  4. Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1. Part 1: ECOG PS 0-1. Part 2: ECOG PS 0-2.

  5. Life expectancy of at least 12 weeks.

  6. Adequate hematologic, hepatic, renal and coagulation functions per protocol.

  7. Male and female subjects of childbearing potential must be willing to completely abstain or agree to use a highly effective method of contraception.

Exclusion criteria

• 1. Any prior therapy targeting CD39, CD73, adenosine A2A receptor, or TGF-β.

  2. Receipt of any investigational agents or devices within 4 weeks prior to the first dose of study drug.

  3. Prior treatment with the following therapies: 1) Anticancer therapy within 30 days or 5 half-lives of the drug prior to the first dose of study drug. At least 14 days must have elapsed between the last dose of prior anticancer agent and the first dose of study drug is administered with certain exceptions. 2) A wash out of at least 2 weeks before the start of study drug for radiation to the extremities and 4 weeks for radiation to the chest, brain, or visceral organs is required.

  4. Prior allogeneic or autologous bone marrow transplantation or solid organ transplantation.

  5. Toxicity from previous anticancer treatment per protocol.

  6. Treatment with systemic immunosuppressive medications within 4 weeks prior to the first dose of study drug.

  7. Subjects who received transfusion of blood products (including platelets or red blood cells), G-CSF, GM-CSF, recombinant erythropoietin, or recombinant thrombopoietin within 14 days prior to the first dose of study treatment.

  8. Major surgery within 4 weeks prior to the first dose of study treatment.

  9. Live vaccine therapies within 4 weeks prior to the first dose of study treatment.

  10. Recent history of allergen desensitization therapy within 4 weeks prior to the first dose of study treatment.

  11. Known allergies to CHO-produced antibodies, which in the opinion of the Investigator suggests an increased potential for an adverse hypersensitivity to ES014.

  12. Invasive malignancy or history of invasive malignancy other than disease under study within the last two years per protocol.

  13. CNS metastases.

  14. Active autoimmune disease or documented history of autoimmune disease that required systemic steroids or other immunosuppressive medications per protocol.

  15. Active interstitial lung disease (ILD) or pneumonitis or a history of ILD or pneumonitis requiring treatment with steroids or other immunosuppressive medications.

  16. Active infection requiring systemic therapy, known human immunodeficiency virus (HIV) infection, or positive test for hepatitis B active infection (HBsAg) or hepatitis C active infection (hepatitis C antibody).

  17. Current active liver or biliary disease with certain exceptions.

  18. History or evidence of cardiac abnormalities per protocol.

  19. History of bleeding tendency or a recent major bleeding event which, in the opinion of the investigator, indicates that the subject is at high risk of receiving study treatment.

  20. Pregnant or nursing females.

  21. Any known, documented, or suspected history of substance abuse that would preclude subject from participation with certain exceptions.

  22. Any other disease or clinically significant abnormality in a laboratory parameter, including serious medical or psychiatric disease/condition, that in the opinion of the investigator may compromise the safety of the subject or the integrity of the study, interfere with the subject's participation in the trial or affect the purpose of the trial.

  23. Those involved in the design and/or implementation of the study.

  24. Those deemed by the investigator to be unable to comply with the steps, limitations and requirements of the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: None (Open label)

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120 participants in 2 patient groups

Part 1 dose escalation

Experimental group

Description:

ES014 doses will be escalated in patients with advanced solid tumors.

Treatment:

Drug: ES014

Part 2 dose expansion

Experimental group

Description:

Part 2 of the study will consist of 4 expansion cohorts at the recommended optimal biological dose determined in Part 1 dose escalation.

Treatment:

Drug: ES014