Study of LM-102 in Subjects in Advanced Tumors

Advanced Solid Tumors Clinical Trial

Official title:

A Phase I, First-in-Human, Open-Label, Dose Escalation Study of LM-102 Injection in Subjects With CLDN18.2-Positive Advanced Solid Tumors

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04735796
• Other study ID #: LM102-01-101
• Status: Terminated
• Phase: Phase 1
• Start date: May 27, 2021
• Est. completion date: May 19, 2022

Study information

• Verified date: October 2022
• Source: LaNova Medicines Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase Ⅰ, first-in-human, open-label, dose escalation study to evaluate the safety and tolerability, PK, immunogenicity and preliminary anti-tumor activity of LM-102 injection in subjects with CLDN18.2-positive advanced solid tumors.

Description:

This is a phase Ⅰ, first-in-human, open-label, dose escalation study to evaluate the safety and tolerability, PK, immunogenicity and preliminary anti-tumor activity of LM-102 injection in subjects with CLDN18.2-positive advanced solid tumors. Dose Escalation Traditional '3+3' escalation design will be used. Dose escalation consists of five ascending dose levels of LM-102 (3 mg/kg, 10 mg/kg, 20 mg/kg, 30 mg/kg and 40 mg/kg). All subjects will be administered every 3 weeks (1 cycle=21 days) with a dose of LM-102 as a 2 h (120±10 min) intravenous (IV) infusion until the disease progression, intolerance, subject discontinuation/informed consent withdrawal, or at the discretion of the investigator in consultation with sponsor. After all the subjects in each cohort complete the DLT assessment, the safety monitor committee (SMC) will make decisions for dose escalations, exploring intermediate/higher doses or terminating dose escalations according to the safety, tolerability, PK and immunogenicity data. The SMC may also adjust the dosage, frequency of administration, PK sample collection plan, etc. Based upon safety, tolerability, PK, and immunogenicity, the MTD or OBD will be determined by SMC. And the RP2D will be determined based on DLTs, MTD or OBD, and the totality of the safety data throughout the study, including dose modifications and delays, PK, and immunogenicity data, etc. The study will consist of 3 periods: 1. Screening period (up to 28 days before the first dose); 2. Treatment period; 3. Follow-up period [28 (±3) days after end of treatment (EOT)/early withdrawal or before other anti-tumor treatments (whichever occurs earlier)]. Safety, tolerability and anti-tumor activity evaluation of LM-102 will be conducted throughout the study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 9
• Est. completion date: May 19, 2022
• Est. primary completion date: May 19, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

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 75 years old, male or female when sign the informed consent form (ICF); 3. Subjects must have histological or cytological confirmation of recurrent or refractory CLDN18.2-positive advanced solid tumors including but not limit to gastric and gastroesophageal junction adenocarcinoma, pancreatic carcinoma, biliary tract carcinoma, colorectal carcinoma, ovarian carcinoma; 4. Subjects are intolerable for available standard therapy or there is no standard available therapy; 5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 with no deterioration within 2 weeks from the first dose; 6. Life expectancy = 3 months; 7. Tumor samples have CLDN18.2 membranous staining in = 1% of the tumor cells with any intensity as determined by central immunohistochemistry (IHC) testing. As such, all patients must be able to provide formalin fixed and paraffin embedded archived tumor tissue samples obtained = 3 years prior to screening;

8. Subjects must have the following organ and marrow function in laboratory tests

within 7 days from the first dose:

1. PLT = 90 × 109/L; ANC = 1.5 × 109/L; Hemoglobin = 9 g/dL, without receiving EPO, G-CSF, or GM-CSF within 14 days and blood transfusion in at least 7 days;

2. Coagulation function: INR = 1.5; APTT = 1.5 × ULN;

3. Liver function: Bilirubin = 1.5 × ULN (Subjects with Gilbert's Syndrome are allowed if direct bilirubin is within normal limits); 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 (using Cockcroft-Gault formula, see Appendix 2); Qualitative urine protein = 1+ or qualitative urine protein = 2+, but 24-hour urine protein < 1g;

5. Cardiac function: Left ventricular ejection fraction (LVEF) = 50%, QT interval (QTcF) = 470 ms.

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

Exclusion Criteria:

1. Subjects who have difficulties in venous blood collection or history of dizziness with blood or needles;

2. Childbearing potential female (see Appendix 3 Contraceptive Methods) who have positive pregnancy test or are breast feeding;

3. Subjects who known to be allergic to LM-102 or any of its excipients;

4. Exposure to any IMP, or participate in any other clinical trial within 28 days prior to 1st dosing LM-102;

5. Subjects with prior anti-tumor within 28 days prior to 1st dosing of LM-102, including radiotherapy (except palliative radiotherapy, beyond 14 days prior to 1st dosing of LM-102, and the toxicity has been recovered as assessed by investigator.), chemotherapy, biotherapy, endocrine therapy and immunotherapy, etc. However, the application of other small molecular targeted drugs and the herbal medicine with anti-tumor indication longer than 14 days or 5 half-life periods of the drug (whichever is longer) is acceptable;

6. Subjects who have received surgical or interventional treatment within 28 days prior to 1st dosing LM-102, excluding operations or surgeries that can be recovered within 14 days prior to 1st dosing LM-102, and have been recovered by the investigator's assessment, e.g., tumor biopsy, puncture, palliative operation, rectal/gastrostomy, etc.;

7. Subjects who have concurrent administration of anticoagulation agents or vitamin K antagonists;

8. Subjects who have concurrent administration of therapeutic doses of heparin (prophylactic doses are acceptable);

9. Subjects who have gastric outlet obstruction, persistent recurrent vomiting or uncontrolled/significant gastrointestinal hemorrhage, symptomatic peptic ulcer, or major bleeding risk in other parts of the body within 28 days prior to 1st dosing LM-102;

10. Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence that the subject's central nervous system metastasis or meningeal metastasis has not been controlled, and the investigator judges it to be unsuitable for inclusion;

11. Subjects who have symptomatic congestive heart failure, history of congestive heart failure greater than New York Heart Association (NYHA) Class II, unstable angina pectoris, uncontrolled hypertension (Blood pressure still = 140/90 mmHg after drug treatment), clinically significant cardiac arrhythmia or myocardial infarction within the past 6 months, etc.;

12. Any adverse events from prior anti-tumor therapy have not yet recovered to = grade 1 of CTCAE v5.0 (Except for some grade 2 toxicity that the investigator judges that there is no safety risk, such as alopecia, and other long term = grade 2 toxicities which would not impact the administration of LM-102 and safety evaluation);

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

14. 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;

15. HIV infection, active HBV infection (HBV DNA exceeds the ULN), active HCV infection (HCV RNA exceeds the ULN);

16. Male and female subjects who are unwilling to use adequate contraceptive methods (e.g, concomitant use of a spermicidal agent, barrier contraceptive, or/and intrauterine contraceptive during the study and for at least 6 months after the last dose of LM-102. (See Appendix 3 for contraceptive methods);

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

18. Subjects who have another active malignancy which is likely to require treatment;

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

Related Conditions & MeSH terms

• Advanced Solid Tumors

Intervention

Drug:
• Drug:LM-102
Traditional '3+3' escalation design will be used. Dose escalation consists of five ascending dose levels of LM-102 (3 mg/kg, 10 mg/kg, 20 mg/kg, 30 mg/kg and 40 mg/kg). All subjects will be administered every 3 weeks (1 cycle=21 days) with a dose of LM-102 as a 2 h (120±10 min) intravenous (IV) infusion until the disease progression, intolerance, subject discontinuation/informed consent withdrawal, or at the discretion of the investigator in consultation with sponsor, at most till by one year.

Locations

Country	Name	City	State
United States	Sarcoma Oncology Research Center, Cancer Center of Southern California	California City	California
United States	Gabrail Cancer and Research Center	Canton	Ohio
United States	Henry Ford Cancer Institute	Detroit	Michigan
United States	University of Texas MD Anderson Cancer Center	Houston	Texas
United States	Indiana University Melvin and Bren Simon Cancer Center	Indianapolis	Indiana
United States	Oklahoma University- Stephenson Cancer Center	Oklahoma City	Oklahoma

Sponsors (1)

Lead Sponsor	Collaborator
LaNova Medicines Limited

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with adverse events and serious adverse events	The safety profile of LM102 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 screening up to 1 year
Primary	Maximum tolerated dose (MTD)	MTD is defined as the highest dose level at which no more than 1 out of 6 subjects experiences a DLT during the first cycle	Cycle 1 of each cohort. Duration of one cycle is 3 weeks
Primary	Dose-limiting toxicities (DLT)	DLT is defined as a toxicity (adverse event at least possibly related to YH002) occurring during the DLT observation period (the initial 21 days)	Cycle 1 of each cohort. Duration of one cycle is 3 weeks
Primary	Change in Vital Signs-ear temperature	Change in vital signs-ear temperature will be measured after the subject has been fully rested.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Change in Vital Signs-pluse rate	Change in vital signs-pluse rate will be measured after the subject has been fully rested.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Change in Vital Signs-blood pressure	Change in vital signs-blood pressure will be measured after the subject has been fully rested.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Change in Electrocardiogram (ECG)-RR interval	RR interval of 12-lead ECG will be performed in the supine position after the patients are fully rested at each timepoint for once. RR is the standard heart rate which calculated by 60 divided by heart rate.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Change in Electrocardiogram (ECG)-QT interval	QT interval of 12-lead ECG will be performed in the supine position after the patients are fully rested at each timepoint for once.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Change in Electrocardiogram (ECG)-QRS duration	QRS duration of 12-lead ECG will be performed in the supine position after the patients are fully rested at each timepoint for once.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Incidence of Abnormal Clinical Laboratory Test Results-hematology	Number of participants with incidence of abnormal clinical lab test results like hematology will be assessed.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Incidence of Abnormal Clinical Laboratory Test Results-Biochemistry	Number of participants with incidence of abnormal clinical lab test results like Biochemistry will be assessed.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Incidence of Abnormal Clinical Laboratory Test Results-Urinalysis	Number of participants with incidence of abnormal clinical lab test results like Urinalysis will be assessed.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Primary	Incidence of Abnormal Clinical Laboratory Test Results-Coagulation test	Number of participants with incidence of abnormal clinical lab test results like Coagulation test will be assessed.	Baseline (Week 0) through approximately 1 year after first administration of LM102
Secondary	Area under the serum concentration versus time curve within one dosing interval (AUCtau)	To determine the pharmacokinetics (PK) profile of LM102	Up to 1 year
Secondary	Volume of distribution (Vd)	To determine the pharmacokinetics (PK) profile of LM102	Up to 1 year
Secondary	Volume of distribution at steady state (Vss)	To determine the pharmacokinetics (PK) profile of LM102	Up to 1 year
Secondary	Maximum serum concentration (Cmax)	To determine the PK profile of LM102 as single agent	Up to 1 year
Secondary	Trough concentration before the next dose is administered (Ctrough)	To determine the PK profile of LM102	Up to 1 year
Secondary	Time to reach maximum serum concentration (Tmax)	To determine the PK profile of LM102	Up to 1 year
Secondary	Clearance (CL)	To determine the PK profile of LM102	Up to 1 year
Secondary	Terminal half-life (T1/2)	To determine the PK profile of LM102	Up to 1 year
Secondary	Dose proportionality	To determine the PK profile of LM102	Up to 1 year
Secondary	Incidence of anti-drug antibodies (ADAs)	To assess the immunogenicity of LM102	Up to 1 year
Secondary	Incidence of neutralizing antibodies (NAbs)	To assess the immunogenicity of LM102	Up to 1 year
Secondary	Objective response rate (ORR)	To assess the preliminary antitumor activity of LM102,The ORR, using RECIST 1.1 criteria, was defined as the percentage of participants in the analysis population who had a confirmed Complete Response (CR; disappearance of all target lesions) or Partial Response (PR; at least a 30% decrease in the sum of diameters of target lesions) at any time during the study, based on Investigator assessment.	Up to 1 year
Secondary	Best of response (BOR)	To assess the preliminary antitumor activity of LM102	Up to 1 year
Secondary	Disease control rate (DCR)	To assess the preliminary antitumor activity of LM102	Up to 1 year