First-in-human Safety and Tolerability of MP0317 in Patients With Relapsed/Refractory Advanced Solid Tumors

Molecular Partners

Status and phase: Terminated; Phase 1

Conditions: Advanced Malignant Solid Tumor

Treatments: Drug: MP0317, a tri-specific fibroblast activation protein (FAP) x CD40 DARPin® drug candidate (q3w regimen); Drug: MP0317, a tri-specific fibroblast activation protein (FAP) x CD40 DARPin® drug candidate (q1w regimen)

Study type: Interventional

Funder types: Industry

Identifiers

NCT05098405

2020-005516-22 (EudraCT Number)

MP0317-CP101

Details and patient eligibility

About

This study is investigating a new experimental therapy, MP0317, a DARPin® drug candidate targeting fibroblast activation protein (FAP) and CD40. Preclinical studies suggest that MP0317 may provide benefit for the treatment of tumors known to express high levels of FAP and for which approved therapies have been exhausted. This is the first study of MP0317 in humans and its main purpose is to test its safety and tolerability in patients with advanced solid tumors. This study will also examine the blood levels of MP0317 at several increasing dose levels and a recommended dose for further development will be determined. The recommended dose will be tested in a second part of the study to confirm safety and to further assess the preliminary biologic and anti-tumor activity.

Enrollment: 46 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Has an advanced, histologically-proven solid tumor of one of the following types, and for which approved therapies have been exhausted or for which the Investigator considers the patient ineligible or unable to tolerate other treatments:

   1. Colorectal cancer
   2. Ovarian cancer
   3. Endometrial cancer
   4. Gastric cancer
   5. Pancreatic cancer
   6. Anal cancer
   7. Cervical cancer
   8. Head and neck squamous cell carcinoma (HNSCC)
   9. Mesothelioma
   10. Prostate cancer
   11. Non-small cell lung cancer (NSCLC)
   12. Melanoma
   13. Urothelial/bladder cancer
   14. Microsatellite instability high cancer of any type
   15. Cutaneous squamous cell cancer
   16. Breast cancer

2. Has signed and dated written informed consent before performing any study procedure, including screening

3. Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 to 1

4. Anticipated life expectancy ≥ 12 weeks by Investigator judgement

5. Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1

6. Should agree to undergo mandatory paired (pre and on-treatment) tumor biopsies and be considered to have biopsiable disease. The biopsies should be performed as follows:

   1. At least 1 tumor lesion ≥ 20 mm amenable to percutaneous biopsy other than the target lesion(s) used to follow response as defined by RECIST v1.1.
   2. For cutaneous or subcutaneous lesions, tumors should be ≥ 5 mm in diameter amenable to biopsy by excisional or punch biopsies without unacceptable risk of a major procedural complication.
   3. For core needle biopsy specimens, at least 3 to 6 cores with an 18-gauge needle should be collected.
   4. The on-treatment tumor biopsy should be taken from the same lesion as the pre-treatment biopsy. The biopsied lesion should be large enough to take both biopsies ≥ 1 cm apart.

7. Should agree to undergo mandatory paired (pre and on-treatment) skin biopsies

8. At least 28 days must have elapsed between any prior major surgery and screening. The following procedures are not considered major:

   1. Obtaining the pre-treatment tumor and skin biopsies as per protocol requirements
   2. Placement of a port for central venous access
   3. Needle, punch or excisional biopsy of a clinically or radiographically detected lesion

9. Laboratory parameters at screening:

   a. Hematology: i. Platelet count ≥ 100,000 cells/mm3 ii. Absolute neutrophil count ≥ 1,000 cells/mm3 iii. Hemoglobin ≥ 9 g/dL b. Serum creatinine < 1.5 x upper limit of normal (ULN) or creatinine clearance > 50 mL/min on the basis of Cockcroft-Gault glomerular filtration rate estimation c. Coagulation: i. International normalized ratio (INR) < 1.5 ii. Prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless therapeutically warranted d. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 3 x ULN e. Bilirubin normal, except for patients with known familial hyperbilirubinemia (such as Gilbert syndrome); for patients with documented Gilbert's syndrome (Gilbert-Meulengracht syndrome) total bilirubin ≤ 3 x ULN is acceptable f. Albumin > 2.8 g/dL or > 28 g/L, and without albumin transfusion for ≥ 7 days before screening

10. Is using highly effective contraception, for females of childbearing potential (FCBP) and for men, as follows:

    1. Female: Is not pregnant, is not breastfeeding, and one of the following applies:

       • Not a FCBP
       • A FCBP who agrees and/or whose male partner agrees to follow the contraceptive guidance from screening, during the treatment period, and for at least 3 months after the last study drug administration. A FCBP must have a negative serum pregnancy test result at screening.

Male: Agreement to use a highly effective contraception method from screening, during the treatment period, and for at least 3 months after the last study drug administration and to refrain from donating sperm during this period.

Exclusion criteria

1. Known hypersensitivity to excipients used in the MP0317 formulation

2. Autoimmune diseases, except autoimmune endocrinopathies that are stable with hormone replacement therapy

3. Inflammatory diseases such as arthritis, colitis, liver fibrosis, cirrhosis, interstitial fibrosis or chronic obstructive pulmonary disease (COPD) that may have elevated tissue fibroblast activation protein (FAP) expression unless approved after consultation with the Sponsor

4. Serious illness or concomitant non-oncological disease considered by the Investigator to be incompatible with participating in the protocol

5. Left ventricular ejection fraction of < 50% on echocardiographic exam or multi-gated acquisition (MUGA) scan at screening

6. History or evidence of clinically significant cardiovascular disease defined as at least one of the following criteria:

   1. Evidence of poorly controlled arterial hypertension (systolic blood pressure > 160 mmHg or diastolic blood pressure > 100 mmHg)
   2. Myocardial infarction or instable angina pectoris within 6 months before screening
   3. Heart failure (New York Heart Association Class III or IV)
   4. Any cardiac arrhythmia that is not well controlled
   5. QT corrected (QTc) prolongation ≥ Grade 2 (> 480 ms) at screening measured on 2 separate electrocardiograms (ECG) at least 10 minutes apart
   6. Clinically significant valvular heart disease

7. Severe dyspnea, pulmonary dysfunction or need for continuous supportive oxygen inhalation

8. Arterial thromboembolic event, stroke or transient ischemia attack within 12 months before screening

9. Known central nervous system (CNS) metastases that are either untreated or are treated but are associated with clinical symptoms (e.g. headache, convulsions); patients with CNS metastases that have been treated with radiotherapy and/or surgery are eligible if they are clinically without symptoms for at least 6 weeks before screening; if under treatment with corticosteroids (not exceeding 10 mg/day prednisone or equivalent) and/or anticonvulsive agents, patients must be on a stable dose for at least 14 days before first study drug administration.

10. Active uncontrolled bleeding or a bleeding diathesis

11. Therapy for active infection needs to be completed at least 7 days before first study drug administration

12. Known positivity for human immunodeficiency virus (HIV) or history of HIV (HIV testing is not mandatory)

13. Active hepatitis B (chronic or acute; HBV) defined as having a positive hepatitis B surface antigen (HBsAg) test at screening. Patients with past or resolved HBV infection (defined as having a negative HBsAg test and a positive hepatitis B core antigen antibody test) are eligible.

14. Active hepatitis C (HCV) infection defined as having a positive HCV antibody test followed by a positive HCV ribonucleic acid (RNA) test at screening. The HCV RNA test will be performed only for patients who have a positive HCV antibody test. Patients who are positive for HCV antibodies are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA.

15. Serious or non-healing wound, skin ulcer or non-healing bone fracture

16. Abdominal fistula, gastrointestinal perforation or intra-abdominal abscess within 6 months before screening

17. Any vaccines within 28 days before first study drug administration

18. An allogenic tissue/solid organ transplant

19. History of another primary malignancy except for:

    1. Malignancy treated with curative intent and with no known active disease ≥ 2 years before screening and of relatively low potential risk for recurrence
    2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of residual disease
    3. Adequately treated carcinoma in situ without evidence of disease
    4. Cancer patients with incidental histologic findings of prostate cancer that, in the opinion of the Investigator, is not deemed to require active therapy (e.g. incidental prostate cancer identified following cystoprostatectomy that is tumor/node/metastasis Stage ≤ pT2N0) may be eligible, pending discussion and approval by the Sponsor

20. Previous treatment with a DARPin® molecule

21. Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) clinical study, or it is the follow-up period of an interventional study

22. Use of an investigational agent within 28 days before first study drug administration

23. Any anticancer treatment, including chemotherapy, hormonal therapy or radiotherapy, within 21 days before first study drug administration; however, the following are allowed:

    1. Hormonal therapy with gonadotropin-releasing hormone (GnRH) agonists or antagonists
    2. Hormone-replacement therapy or oral contraceptives
    3. Palliative radiotherapy for bone metastases within 14 days before first study drug administration

24. Continuous corticosteroid use exceeding 10 mg/day prednisone or equivalent

25. Any condition that, in the opinion of the Investigator, would interfere with evaluation of the investigational medicinal product (IMP) or interpretation of the patient's data

26. Unable or unwilling to comply with all study requirements for clinical visits, examinations, tests and procedures

27. Patient deprived of liberty by a judicial or administrative decision, patient admitted to a social institution or who is under a measure of legal protection, patient hospitalized without consent or who is in an emergency situation

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Sequential Assignment

Masking: None (Open label)

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46 participants in 2 patient groups

Dose-escalation Cohorts (q3w)

Experimental group

Description:

The starting dose is 0.03 mg/kg every 3 weeks (q3w) and up to 6 dose levels are planned. Study treatment will be administered as an intravenous (IV) infusion until progressive disease (PD), unacceptable toxicity, withdrawal of consent or other reasons to discontinue treatment occur, whichever comes first.

Treatment:

Drug: MP0317, a tri-specific fibroblast activation protein (FAP) x CD40 DARPin® drug candidate (q3w regimen)

Dose-escalation Cohorts (q1w)

Experimental group

Description:

The starting dose is 0,5 mg/kg every week (q1w) and up to 3 dose levels are planned. Study treatment will be administered as an intravenous (IV) infusion until progressive disease (PD), unacceptable toxicity, withdrawal of consent or other reasons to discontinue treatment occur, whichever comes first.

Treatment:

Drug: MP0317, a tri-specific fibroblast activation protein (FAP) x CD40 DARPin® drug candidate (q1w regimen)