Study of LM-302 in Patients With Advance Solid Tumors

Advanced Solid Tumor Clinical Trial

Official title:

A Phase I/II , Open, Multicentre, Dose-escalation and Expansion Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Antitumour Activity of LM-302 in Patients With CLDN18.2 Positive Advanced Solid Tumours

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05161390
• Other study ID #: LM302-01-102
• Status: Active, not recruiting
• Phase: Phase 1/Phase 2
• Start date: November 26, 2021
• Est. completion date: June 8, 2025

Study information

• Verified date: April 2024
• Source: LaNova Medicines Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase I/II Study of LM-302 in Patients with CLDN18.2-Positive Advanced Solid Tumors

Description:

A Phase I/II, First-in-Human, Open-Label, Dose Escalation and Expansion Study of LM-302 in Patients with CLDN18.2-Positive Advanced Solid Tumors The study includes phase I (dose escalation) to determine MTD/RP2D and phase II (dose expansion) to assess the preliminary anti-tumor activity, etc..

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 206
• Est. completion date: June 8, 2025
• Est. primary completion date: March 10, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

Subjects will be enrolled into the study only if they meet all of the following 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 document prior to any procedure;

2. Aged between 18 to 80 years old, male or female when sign the Informed consent form (ICF);

3. ECOG score 0-1;

4. Life expectancy = 3 months;

5. Subjects have histological or cytological confirmation of advanced solid tumors, and are intolerable for available standard therapy, or there is no available standard therapy;

6. Claudin18.2(CLDN18.2) status will be tested by immunohistochemistry (IHC) by central lab, the result must be positive;

7. At least one evaluable lesion for phase I and one measurable lesion for phase II according to RECIST v1.1;

8. Subjects must have the following organ and marrow function in laboratory tests within 7 days prior to the first dose;

9. Subjects who are able to well communicate with investigators as well as understand and adhere to the requirements of this study. Exclusion Criteria:

Subjects will be excluded from the study, if they meet any of the following criteria:

1. Participate in any other clinical trial within 28 days prior to 1st dosing of LM-302;

2. Subjects with anti-tumor treatment within 21 days prior to 1st dosing of LM-302, including radiotherapy, chemotherapy, biotherapy, endocrine therapy and immunotherapy, etc.

3. Any adverse event from prior anti-tumor therapy has not yet recovered to =grade 1 of CTCAE v5.0;

4. Peripheral sensory or motor neuropathy = grade 2;

5. Subjects with uncontrolled tumor-related pain;

6. Subjects with known central meningeal metastasis;

7. Subjects with known brain metastasis, stable brain metastasis judged by investigator can be included;

8. Subjects with uncontrolled third interstitial effusion judged by the investigator to be unsuitable for inclusion;

9. Subjects with known antibody drug allergy = grade 3;

10. Subjects who have received the treatment with ADCs targeting to CLDN18.2;

11. Subjects who were intolerable to the treatment with MMAE based ADCs or anti-CLDN18.2 antibodies are not eligible;

12. Administrate strong inhibitors/strong inducers of CYP3A4 within 14 days prior to 1st dosing of LM-302;

13. Use of any live vaccines within 28 days prior to 1st dosing of LM-302;

14. Subjects with the history of interstitial lung disease or drug-induced interstitial lung disease/pneumonitis;

15. Subjects who are taking therapeutic doses of anticoagulants such as heparin or vitamin K antagonists (except preventive treatment at a stable dose);

16. Uncontrolled persistent and recurrent vomiting (e.g. due to gastric outlet obstruction);

17. Subjects with uncontrolled/severe gastrointestinal hemorrhage, or ulcer within 28 days prior to 1st dosing of LM-302;

18. Subjects who have received surgical or interventional treatment within 28 days prior to 1st dosing LM-302, with the exception for tumor biopsy,puncture, etc.;

19. (Limited Phase? dose expansion)Subjects who have another active malignancy which is likely to require treatment, and have the history of another malignancy within 2 years before the 1st dosing LM-302;

20. Subjects who have severe cardiovascular disease;

21. Subjects who have uncontrolled or severe illness, including but not limited to ongoing or active infection requiring antibiotics administration;

22. 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;

23. HIV infection, active HBV and HCV infection;

24. Child-bearing potential female who have positive results in pregnancy test before the 1st dosing LM-302 or are lactating;

25. Subjects who have psychiatric illness or social situations that would preclude study compliance;

26. Subject who is determined as not eligible to participate in this study by the investigator.

Related Conditions & MeSH terms

• Advanced Solid Tumor
• Neoplasms

Intervention

Drug:
• LM-302 Injection
LM-302 Injection with dose escalation stage of different dose levels, as well as dose expansion stage with recommended dose level from dose escalation stage.

Locations

Country	Name	City	State
China	Shanghai East Hospital	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
LaNova Medicines Zhejiang Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose limiting toxicity (DLT)	DLT is defined as a toxicity (adverse event at least possibly related to LM302) occurring during the DLT observation period	Cycle 1 of each cohort. Duration of one cycle is 21 days
Primary	Adverse Events and Serious Adverse Events	The safety profile of LM-302 will be assessed by monitoring the adverse events (AE) per the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v5.0	From signing the ICF until 28 days after EOT or accept other anti-cancer therapy
Primary	Recommended Phase II Dose (RP2D)	The RP2D will be determined during the dose expansion stage of the study. RP2D will be determined using available safety and efficacy data	up to 21 days following first dose
Primary	Maximum Tolerated Dose (MTD)	The MTD is defined as the dose of which the toxicity rate during the DLT observation period (21 days after the first administration in cycle 1 on day 1).	up to 21 days following first dose
Secondary	Area under plasma concentration vs time curve (AUC) for LM-302	changes in AUC over time in participants with LM-302	Up to finished cycle 5 (each cycle is 21 days)