Treatment for advanced and metastatic solid tumors using MIL97

A Phase I Multicenter, Open Label, Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of MIL97 in Subjects With Advanced or Metastatic Solid Tumors

This study is testing a new treatment called MIL97 to see if it can safely help people with advanced or metastatic solid tumors.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 62 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: Beijing Mabworks Biotech Co., Ltd. (Industry-sponsored)
• Drugs / interventions: chemotherapy, immunotherapy
• Locations: 1 site (Beijing, Beijing Municipality)
• Trial ID: NCT04965077 on ClinicalTrials.gov

What this trial studies

This Phase 1 clinical trial is a global, multi-center, open-label study designed to evaluate the safety, tolerability, pharmacokinetics, biomarkers, and efficacy of MIL97 in patients with advanced or metastatic solid tumors. The study includes a dose escalation phase with an accelerated titration design followed by a 3+3 dose-escalation design, starting at a dose of 0.01 mg/kg administered every three weeks. Participants will be monitored for dose limiting toxicity and may be assigned to either a two-week or three-week treatment regimen based on initial findings. The trial aims to identify effective dosing strategies for further exploration in a larger cohort.

Who should consider this trial

Good fit: Ideal candidates for this study are adults aged 18 and older with refractory or relapsed metastatic and/or unresectable solid tumors.

Not a fit: Patients with significant comorbidities that could interfere with therapy or those with recent serious cardiovascular events may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with advanced or metastatic solid tumors who have limited treatment alternatives.

How similar studies have performed: While this approach is novel, similar studies involving monoclonal antibodies have shown promise in treating advanced solid tumors.

Eligibility criteria

Inclusion Criteria:

1. Adult patients, \>=18 years of age;
2. Diagnosis of Refractory/relapsed metastatic and/or unresectable solid tumors;
3. At least one extracranial measurable unirradiated lesion or evaluable lesion (recist v1.1) ;
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1Life expectancy \>=3 months;
5. Sufficient organ and bone marrow function within 7 days before enrollment;
6. Life expectancy \>=12 weeks;
7. Able and willing to provide written informed consent and to comply with the study protocol.

Exclusion Criteria:

1. have a history of myocardial infarction within 6 months or a history of arterial thromboembolic event within 3 months before the first dose;
2. Comorbidity that would interfere with therapy, including interstitial pneumonia, symptomatic congestive heart failure; unstable angina, uncontrolled hypertension; ongoing cardiac arrhythmia ≥ CTCAE 5.0 Grade 3, active coagulopathy, uncontrolled diabetes, QTcF\>450ms (Male) or QTcF\>470ms (Female) at screening;
3. Patients have a known or suspected history of an autoimmune disorder, except for the following: Type 1 diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders such as vitiligo, or alopecia not requiring systemic therapy, or conditions not expected to recur in the absence of an external trigger are eligible;
4. Have a history of manifested central nervous system (CNS) metastases or have primary brain tumor. Patients with known or suspected leptomeningeal disease or cord compression;
5. Receipt of allograft or allogeneic hematopoietic stem cell transplantation;
6. Patients have another active invasive malignancy, but history of a non-invasive malignancy and history of malignancy that is in complete remission after treatment with curative intent are allowed;
7. Active known clinically serious infections are required intravenous antibiotic treatment;
8. Have a history of primary immunodeficiency, including but not limited with human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness;
9. Active and clinical significant bacterial, fungal, or viral infection including hepatitis B virus (HBV) or hepatitis C (HCV) (Hepatitis B should be confirmed as HBV surface antigen (HBsAg) positive or HBV core antibody (HBcAb) positive with HBV DNA above ULN);
10. Any antitumor therapy within prior 4 weeks (including chemotherapy, targeted therapy, hormone therapy, immunotherapy, radiotherapy, tumor embolization, etc), except for palliative radiotherapy for relief bone pain;
11. Major surgery within prior 4 weeks or expected to require major surgery during study treatment (Major surgery: laparotomy, thoracotomy, and internal organs excision by laparoscopic surgery);
12. Patients have concurrent received or used an immunosuppressive agent within 14 days before study treatment, with the following exceptions and notes: Systemic steroids at physiologic doses, intranasal, inhaled, topical, intra-articular, and ocular corticosteroids with minimal systemic absorption, transient courses of steroids may be approved by the Medical Monitor;
13. Previous exposure to CD40 antibodies;
14. Patients received a live attenuated vaccine within 28 days before study treatment and plan to receive live vaccines during the study unless approved by both investigator and sponsor;
15. Toxicities due to prior therapy are unresolved to ≤ CTCAE 5.0 Grade 1 except for AEs not constituting a safety risk to the patient based on the judgment of investigators;
16. History of clinically significant sensitivity or allergy to MIL97, their excipients, or intravenous gamma globulin;
17. Females who are pregnant or lactating or who intend to become pregnant during the clinical trial period and within 6 months after discontinuation of study treatment. Female or Male who refused using birth control during the clinical trial period and within 6 months after discontinuation of study treatment;
18. Participation in a therapeutic clinical study within 4 weeks for biological treatments, and within 1 week or 5 half-lives for small-molecule agents, before study drug treatment, or current participation in other therapeutic investigational procedures;
19. Patients who have any clinically significant psychiatric, social, or medical condition that, in the opinion of the investigator, could increase the patient's risk, interfere with protocol adherence, or affect the patient's ability to give informed consent are ineligible to participate in the study.

Where this trial is running

Beijing, Beijing Municipality

• Chinese PLA General Hospital — Beijing, Beijing Municipality, China (Recruiting)

Study contacts

• Study coordinator: Jianming Xu, Ph.D

Conditions Advanced or Metastatic Solid Tumor