A Phase 2, Open-Label Study to Evaluate the Safety and Effects of HLX-1502 in Patients With Neurofibromatosis Type 1

Trial Title: A Phase 2, Open-Label Study to Evaluate the Safety and Effects of HLX-1502 in Patients With Neurofibromatosis Type 1

NCT ID: NCT06541847

Condition: Neurofibromatosis Type 1

Conditions: Official terms:
Neurofibromatoses
Neurofibromatosis 1
Neurofibroma

Conditions: Keywords:
Neurofibromatosis Type 1
Plexiform Neurofibroma

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: HLX-1502
Description: Participants will take an oral dose three times a day (with or without food) for up to 24 cycles (A cycle is defined as 28 days)
Arm group label: HLX-1502

Summary: The trial will be an open label, single arm, phase 2 study in 20 participants. The study will assess the tolerability and efficacy of HLX-1502 in participants with NF1 16 years of age or older with progressive and/or symptomatic PN.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. All participants must have a diagnosis of NF1 based on the 2021 revised consensus criteria. 2. Participants must have PN(s) that are progressive OR are causing significant morbidity, such as (but not limited to) head and neck lesions that are compromising the airway or great vessels, brachial or lumbar plexus lesions that are causing nerve compression and loss of function, lesions causing significant disfigurement (e.g., orbital lesions), lesions of the extremity that cause limb hypertrophy or loss of function, and painful lesions. Participants with paraspinal PN will be eligible for this trial. Histologic confirmation of tumor is not necessary but should be considered if there are clinical or radiographic findings concerning for malignant transformation of a PN. 3. Measurable Disease: Participants must have measurable PN(s) amenable to volumetric MRI analysis. For the purpose of this study, the target lesion must be seen on at least 3 consecutive MRI slices and the field of view must contain the entire tumor of interest. Tumors must be at least 3 mL in volume (most PN 3 cm in longest diameter will meet this criteria). If the tumor is < 3 cm in longest diameter, the participant may still be eligible. Central review of the MRI of the target PN is required prior to enrollment to ensure that the tumor is measurable and amenable to volumetric analysis. 4. Age: Participants must be ≥ 16 years of age at the time of study entry. Note: Patients < 18 years of age should be counseled on the availability of MEKi therapy, and enrolled only if patients have failed MEKi therapy, had to come off MEKi therapy due to toxicity, or have a contraindication to MEKi therapy. 5. Weight ≥ 49 kg 6. Performance Level: Participants must have Karnofsky greater ≥ 50% 7. Organ Function Requirements: Adequate Bone Marrow Function, Adequate Renal Function, Adequate Liver Function, Normal pancreatic function and Systolic blood pressure ≤ 130 mmHg and a diastolic pressure of ≤ 80 mmHg in an average of 3 measurements, 5 minutes apart. 8. Sexually active women of childbearing potential and fertile male participants and their partners must agree to use effective methods of contraception e.g., hormonal oral contraception, injectables, intrauterine device, surgical sterilization including vasectomy, or hormonal implant with barrier methods (male condom, female condom, or diaphragm with spermicidal gel) during the course of the study and for 4 months after the last dose of study treatment. Barrier methods alone are insufficient. True sexual abstinence or evidence of surgical sterility (e.g. vasectomized partner, post-hysterectomy, menopause with last menstrual period >=12 months prior to screening visit) are acceptable method of birth control. Persons of childbearing potential will be given a pregnancy test within 14 days prior to first dose of study treatment and must have a negative urine or serum pregnancy test. 9. The participant is not planning to undergo surgery or other interventions/treatments for the target lesion, except protocol specified therapy, for the duration of the study. 10. The participant or the participant's legal authorized representative is able to understand the informed consent form describing the risks of the study and voluntarily signs the informed consent document. 11. In the opinion of the investigator, the participant is willing and able to attend study visits, comply with the study procedures as specified in the protocol, and comply with the administration of the study drug. Exclusion Criteria: 1. Prior treatment with HLX-1502 for a PN. 2. The participant has used any of the following systemic medications/therapies within the specified period prior to enrollment: MEK-inhibitors, other drugs in the TKI class, HLX-1502, Myelosuppressive chemotherapy, Hematopoietic growth factors, Biologic (anti-neoplastic agent), Investigational Drugs, Any other systemically administered anti-neoplastic agent and Radiation therapy. 3. Participants with high-grade glioma, malignant peripheral nerve sheath tumor, or other malignancy who received treatment in the last 12 months. Exceptions include basal cell carcinoma of the skin and squamous cell carcinoma of the skin that have undergone potentially curative therapy. If the investigator has any clinical concerns for ANNUBP/Atypical Neurofibroma or MPNST, a biopsy sample must be taken prior to study confirming eligibility. 4. Dental braces or prosthesis that interfere with volumetric analysis of the neurofibroma(s). 5. Surgery: Any major surgery within 12 weeks before starting the Treatment Period or foreseen during participation in the trial and any minor surgeries within 1 month before first dose of study treatment. 6. Ophthalmologic conditions 7. Cardiovascular disorders 8. Other clinically significant disorders that would preclude safe study participation, including active infection, a known history of HIV seropositivity or known immunodeficiency or Known history of Hepatitis B or Hepatitis C. 9. Participants who require treatment with a drug that is a substrate of CYP1A2, CYP2C8, UGT1A1, UGT1A3 with a narrow therapeutic index (Appendix VII) during protocol therapy. 10. Known severe sensitivity to HLX-1502 or any excipient of HLX-1502 or history of allergic reactions attributed to compounds of similar chemical or biologic composition to HLX-1502. 11. Known severe sensitivity to FD&C Yellow No. 5 (tartrazine). 12. Participants receiving therapeutic anticoagulation with vitamin K antagonist (VKA e.g. warfarin, acenocoumarol, phenprocoumon) 13. Participants presently with iron deficiency and/or actively receiving iron replacement or requiring treatment with copper or zinc for any indication at study baseline. 14. Pregnant or breast-feeding women 15. Unable or unwilling to swallow tablets. 16. Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter ingestion and/or the absorption of HLX-1502 17. Participants who have other medical, social or concurrent challenges that are likely to negatively impact their ability to meet all of the trial obligations and therefore may increase the risk of safe participation in the study.

Gender: All

Minimum age: 16 Years

Maximum age: N/A

Healthy volunteers: No

Start date: October 2024

Completion date: November 2027

Lead sponsor:
Agency: Healx Limited
Agency class: Industry

Source: Healx Limited

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06541847