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Study of LaNova Medicines(LM)-302 in Combination With Toripalimab in Patients With Advanced Solid Tumors

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT05188664
Recruitment Status : Enrolling by invitation
First Posted : January 12, 2022
Last Update Posted : May 23, 2022
Sponsor:
Information provided by (Responsible Party):
LaNova Medicines Limited ( LaNova Australia Pty Limited )

Brief Summary:
A Phase I/II, Open-Label, Multiple Centre Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Preliminary Efficacy of LM- 302 in Combination with Toripalimab in Patients with Advanced Solid Tumors

Condition or disease Intervention/treatment Phase
Advanced Solid Tumor Drug: LM-302 Drug: Toripalimab Phase 1 Phase 2

Detailed Description:
This is a study of LM-302 in combination with toripalimab in patients with advanced solid tumors .The study includes phase I (dose escalation) and phase II (dose expansion). All participants enrolled in the study will be administered every 3 weeks (1 cycle=21 days) with a dose of LM-302 intravenous infusion followed by toripalimab intravenous infusion on day 1 until meet the criteria of treatment discontinuation or withdraw, whichever occurs earlier.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: This study includes two stages, Phase I (Dose escalation) which includes LM-302 monotherapy dose escalation (part Ia) and LM-302 in combination with Toripalimab therapy dose escalation (part Ib) and Phase II (Dose expansion).
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase I/II, Open-Label, Multiple Centre Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Preliminary Efficacy of LM- 302 in Combination With Toripalimab in Patients With Advanced Solid Tumors
Actual Study Start Date : May 10, 2022
Estimated Primary Completion Date : October 1, 2023
Estimated Study Completion Date : March 1, 2024

Arm Intervention/treatment
Experimental: LM-302 monotherapy dose escalation
LM-302 monotherapy dose escalation (part Ia). Accelerated titration combined with traditional 3+3 design will be used for monotherapy dose escalation (part Ia).
Drug: LM-302
LM-302 is given by intravenous (IV) infusion on day 1 every 3 weeks。

Experimental: LM-302 in combination therapy dose escalation
LM-302 in combination therapy dose escalation (part Ib).Accelerated titration combined with traditional 3+3 design will be used for LM-302 in combination with fixed dose Toripalimab dose escalation (part Ib).
Drug: LM-302
LM-302 is given by intravenous (IV) infusion on day 1 every 3 weeks。

Drug: Toripalimab
Toripalimab with a fixed dose is given by intravenous (IV) infusion on day 1 every 3 weeks.

Experimental: LM-302 Dose Expansion
SMC will select appropriate dose(s) and/or tumor types for dose expansion study.
Drug: LM-302
LM-302 is given by intravenous (IV) infusion on day 1 every 3 weeks。

Drug: Toripalimab
Toripalimab with a fixed dose is given by intravenous (IV) infusion on day 1 every 3 weeks.




Primary Outcome Measures :
  1. DLT [ Time Frame: Cycle 1 of each cohort. Duration of one cycle is 21 days ]
    To assess the safety and tolerability for LM-302 in combination with toripalimab in subjects with advanced solid tumors.

  2. RP2D [ Time Frame: Up to 6 months ]
    Obtain the recommended phase 2 dose (RP2D) for LM-302 in combination with toripalimab in subjects with advanced solid tumors.

  3. OBD [ Time Frame: Up to 6 months ]
    Obtain the optimal biologic dose (OBD) for LM-302 in combination with toripalimab in subjects with advanced solid tumors.

  4. MTD [ Time Frame: Up to 21 days ]
    Obtain the Maximum Tolerated Dose (MTD) for LM-302 in combination with toripalimab in subjects with advanced solid tumors.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Subjects who are fully informed of the purpose, nature, method and possible adverse reactions of the study, and are willing to participate in the study and sign the informed consent form (ICF) prior to any procedure.
  2. Aged ≥18 years old when sign the ICF, male or female.
  3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1, and no deterioration within 2 weeks prior to the first dose.
  4. Life expectancy ≥ 3 months.
  5. Subjects must have histological or cytological confirmation of recurrent or refractory advanced solid tumors, and have progressed on standard therapy, or are intolerable for available standard therapy, or there is no available standard therapy.
  6. CLDN18.2 test should be performed for the enrolled subjects if the archived tumor tissue samples are available.
  7. At least one measurable lesion for phase II dose expansion, according to RECIST v1.1 as assessed by the investigator.
  8. Subjects must show appropriate organ and marrow function in laboratory examinations within 7 days prior to the first dose:

    1. Bone marrow reserve: Platelet count (PLT) ≥ 90 × 109/L; Absolute neutrophil count (ANC) ≥ 1.5 × 109/L; Haemoglobin ≥ 9 g/dL, without receiving EPO, G-CSF, or GM-CSF within 14 days and blood transfusion including red blood cell and platelet transfusion in at least 7 days prior to first dose.
    2. Coagulation function: INR ≤ 1.5; APTT ≤ 1.5 × ULN.
    3. Liver function: Total bilirubin ≤ 1.5 × ULN (Subjects with Gilbert's Syndrome are allowed if total bilirubin ≤ 3 × ULN); AST and ALT ≤ 2.5 × ULN without liver metastases (≤ 5 × ULN if liver metastases are present); Albumin ≥ 2.5 g/dL.
    4. Kidney function: Serum creatinine ≤ 1.5 × ULN, or creatinine clearance ≥ 50 mL/min.
    5. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%; QT interval (QTcF) ≤ 480 ms.
  9. Subjects who are able to communicate well with investigators and understand and adhere to the requirements of this study.

Exclusion Criteria:

  1. Participate in any other clinical trial within 28 days prior to 1st dosing of investigational medicinal product (IMP).
  2. Subjects with anti-tumor treatment within 21 days prior to 1st dosing of IMP, including radiotherapy, chemotherapy, biotherapy, endocrine therapy and immunotherapy, etc. the following treatments have different time limits:

    1. Local small-scale palliative radiotherapy (bone metastasis radiotherapy to control pain) within 14 days prior to 1st dosing.
    2. Oral anti-tumor therapy, including fluorouracil antitumor drugs and small molecular targeted drugs, etc. within 14 days or 5 half-lives of the drug (whichever is longer) prior to 1st dosing.
    3. Traditional herbal medicine with anti-tumor indication within 14 days prior to 1st dosing.
    4. Nitrosourea or Mitomycin C within 42 days prior to 1st dosing.
  3. Subjects who experienced grade 3 or higher hypersensitivity to the treatment that contains monoclonal antibody, e.g., monoclonal antibody therapy, ADC etc.
  4. Subjects who were intolerable to the treatment with MMAE based ADCs or anti-CLDN18.2 antibodies, but they can be enrolled if they were tolerable to the treatments and have experienced a 28-day's washout period prior to 1st dosing of IMP.
  5. Subjects who were intolerable to the immunotherapy targeting PD-1 receptor, or its ligand PD-L1.
  6. Any adverse event from prior anti-tumor therapy has not yet recovered to ≤ grade 1 of CTCAE v5.0.
  7. Administrate strong inhibitors/strong inducers of CYP3A4 within 14 days prior to 1st dosing of IMP.
  8. Subjects who take systemic corticosteroids (> 10 mg daily prednisone equivalents) or other systemic immunosuppressive medications.
  9. Pre-existing peripheral sensory or motor neuropathy ≥ Grade 2.
  10. Subjects with uncontrolled pain. Subjects requiring analgesic treatment must be on a stable regimen before participating in the study.
  11. Subjects with known central nervous system (CNS) or meningeal metastasis.
  12. Subjects who have uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures.
  13. Subjects with known active keratitis or corneal ulcerations.
  14. Use of any live attenuated vaccines within 28 days prior to 1st dosing of IMP.
  15. Subjects with the history of idiopathic pulmonary fibrosis, organizing pneumonia.
  16. Subjects with the known history of autoimmune disease.
  17. Subjects who are taking therapeutic doses of anticoagulants.
  18. Subjects with gastric outlet obstruction, persistent recurrent vomiting or uncontrolled/severe gastrointestinal hemorrhage, or ulcer within 28 days prior to 1st dosing of IMP.
  19. Subjects who received major surgery or interventional treatment within 28 days prior to 1st dosing of IMP.
  20. Subjects who have other active malignancies which are likely to require the treatment.
  21. Subjects who have severe cardiovascular disease.
  22. Subjects who have uncontrolled or severe illness, including but not limited to ongoing or active infection (e.g., active COVID-19/SARS-CoV-2 infection, etc.) requiring therapeutic antibiotics and/or other administration, while SARS-CoV-2 testing is not mandatory for study entry, and the testing should follow local clinical practice guidelines/standards.
  23. Subjects who have a history of immunodeficiency disease, including other acquired or congenital immunodeficiency diseases, or organ transplantation, or allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation.
  24. HIV infection, active HBV and HCV infection.
  25. Child-bearing potential female who have positive results in pregnancy test or are lactating.
  26. Subjects who have psychiatric illness or disorders that may preclude study compliance; Subject who is judged as not eligible to participate in this study by the investigator.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05188664


Locations
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Australia
The Alfred
Melbourne, Australia
Sponsors and Collaborators
LaNova Australia Pty Limited
Investigators
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Principal Investigator: Vinod Ganju Peninsula & South Eastern Haematology and Oncology Group
Principal Investigator: Ben Markman The Alfred
Principal Investigator: Sophia Frentzas Monash Medical Centre Clayton
Principal Investigator: Sara Wahlroos Chris O'Brien Lifehouse
Principal Investigator: Jessica Smith Macquarie University
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Responsible Party: LaNova Australia Pty Limited
ClinicalTrials.gov Identifier: NCT05188664    
Other Study ID Numbers: LM302-01-201
First Posted: January 12, 2022    Key Record Dates
Last Update Posted: May 23, 2022
Last Verified: May 2022
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Neoplasms