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Study to Evaluate the Safety, Tolerability, PK Characteristics and Anti-tumor Activity of FCN-159 in Adult and Pediatric Participants With Neurofibromatosis Type 1

Primary Purpose

Neurofibromatosis 1, Plexiform Neurofibroma, NF1

Status
Active
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
FCN-159
Sponsored by
Shanghai Fosun Pharmaceutical Industrial Development Co. Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neurofibromatosis 1

Eligibility Criteria

2 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

General inclusion criteria for Phase I and II:

1.Cohort 1: 16-70 years of age (inclusive) with a body weight of ≥ 94 lbs or 42.5 kg.

Cohort 2: 2-15 years of age (inclusive) and able to swallow whole tablet. 2.Participants must be diagnosed with NF1-related plexiform neurofibromas (PN) and symptomatic with requirement of systematic therapy per investigator's judgment. A PN is defined as a neurofibroma that has grown along the length of a nerve and may involve multiple fascicles and branches. A spinal PN involves two or more levels with connection between the levels or extending laterally along the nerve. Diagnosis of neurofibromatosis type 1 (NF1) is based on meeting at least 1 of the following 2 diagnostic criteria:

  1. Genetic testing confirmation: i.e., positive for NF1 germline mutation per CLIA-certified laboratory (or equivalent) testing. Note: NF1 germline mutation positive must either be confirmed by the FCN-159-002 central laboratory or have documentation of NF1 mutation issued by a CLIA-certified laboratory (or equivalent) - OR -
  2. Clinical and imaging confirmation: Meets at least 2 of the following 7 NF1 diagnostic criteria according to the clinical NIH consensus criteria:

    1. ≥ 6 cafe-au-lait macules (>0.5 cm in prepubertal participants and > 1.5 cm in post-pubertal participants);
    2. Axillary freckling or freckling in inguinal regions;
    3. ≥2 neurofibromas of any type, or ≥ 1 plexiform neurofibroma;
    4. An optic pathway glioma;
    5. ≥2 Lisch nodules (iris hamartomas);
    6. A distinctive bony lesion such as dysplasia of the sphenoid bone or dysplasia or thinning of long bone cortex);
    7. First-degree relative with NF1. 3. Participants should meet one of the following criteria
    1. Must be judged by the investigator to be inoperable for complete resection without causing substantial damage, or unsuitable for surgery with high surgical risks or patient refuses surgery, e.g. due to encasement of or close proximity to vital structures, invasiveness, or high vascularity. NF1 has to cause or has the potential to cause significant morbidity, such as (but not limited to) head and neck lesions that could compromise the airway or great vessels, paraspinal lesions that can cause myelopathy, brachial or lumbar plexus lesions that could cause nerve compression and loss of function, lesions that could result in major deformity (e.g., orbital lesions) or are significantly disfiguring, lesions of the extremity that cause limb hypertrophy or loss of function, and painful lesions.
    2. The participants who have previously received surgical treatment, if the PN resection is incomplete, the postoperative residual exceeds 15% of the primary lesion, or relapse after surgery, and the lesions of at least 3 cm are measured in one dimension, are eligible for enrollment. At least a 28-day interval is required between surgery and the first dose of FCN-159.

      4. Participants must have a measurable lesion, defined as at least 3 cm in length in at least one dimension, amenable to MRI for efficacy assessment.

      5. Adult participants: Karnofsky performance level of ≥70%; Pediatric participants: Lansky performance score ≥ 70%, see Appendix 18.

      Note: Participants who are wheelchair bound because of paralysis secondary to a plexiform neurofibroma should be considered ambulatory when they are in the wheelchair. Similarly, participants with limited mobility secondary to the need for mechanical support (such as an airway PN requiring tracheostomy or CPAP) will also be considered ambulatory for the purposes of this study.

      6. Coagulation function: International normalized ratio (INR) and activated partial thromboplastin time (APTT) ≤ 1.5 ULN.

      7. Participants or their legal guardians (if the participant is <18 years old) are able to understand and voluntarily sign a written informed consent form.

      8. For participants of childbearing potential: participants must agree to take effective contraception, and receive double barrier contraception, condom, oral or injectable contraceptives, intrauterine device and other contraceptive methods during treatment and for at least 90 days after the last dose. Male participants must agree to avoid sperm donation for at least 90 days after the last dose.

      9. Willing to avoid excessive sun exposure and use adequate amounts of sunscreen if sun exposure is anticipated.

      Exclusion Criteria:

      Participants who meet any of the following conditions shall not be included in this clinical study:

      Exclusion criteria for Phase I and II:

      1. Participants who have previously received one of the following:

        1. Chemotherapy for NF1 within 3 months of enrollment. Ongoing side effects of that treatment > Grade 1 (except alopecia).
        2. Treatment with any drug or biologic therapy within 14 days of starting FCN-159, such as: tipifarnib, pirfenidone, Peg-Interferon, sorafenib or other VEGFR inhibitors
        3. Strong CYP3A4, CYP2C8 and CYP2C9 inhibitors or inducers (moderate inducers for CYP2C8 and CYP2C9) within 14 days before treatment of the study drug, except for topical skin use.
        4. Use of growth factors to increase the number or function of platelets or white blood cells within 7 days before administration of FCN-159.
        5. Radiotherapy, surgery or immunotherapy within 4 weeks before administration of FCN-159.
        6. Participation in other interventional clinical trials within 4 weeks before administration of FCN-159.
        7. Prior treatment with selumetinib or any other MEK 1/2 inhibitors (specific for phase 2 part).
      2. Participants with malignant tumors associated with NF1 requiring chemotherapy, radiotherapy, or surgery, such as intermediate- to high-grade optic gliomas or malignant peripheral nerve sheath tumors.
      3. Patients have other malignant tumor history or with other malignant tumors simultaneously (excluding cured non-melanoma skin basal cell carcinoma, breast carcinoma in situ or cervix cancer in situ, and other malignant tumors without disease evidence for the past 5 years);
      4. Participants who are unable to undergo MRI examination and/or for whom MRI examination is contraindicated (e.g., due to prostheses, orthotics or dental appliances or due to interference with volumetric analysis of target PN on MRI).
      5. Uncontrolled hypertension (despite medical therapy)

        • Adult participants: defined as systolic or diastolic blood pressures > 140/90 mmHg on repeat examination with existing anti-hypertension therapy.
        • Pediatric participants: Blood pressure (BP) greater than or equal to the 95th percentile for age, height, and gender measured as described in (Appendix 19).
      6. Participants with dysphagia, active digestive diseases, malabsorption syndrome, or other conditions that might affect the absorption of the study drug.
      7. Previous or current retinal vein occlusion (RVO), retinal pigment epithelial detachments (RPED), glaucoma and other significant abnormality in ophthalmic examination.
      8. Interstitial pneumonia, including existing clinically significant radiation pneumonitis.
      9. Cardiac dysfunction or concomitant diseases meeting any one of the following conditions will be excluded:

        1. Three 12-lead electrocardiogram (ECG) measurements performed at the study site during the screening period for which the mean value of three measurements was calculated according to the QTcF formula using the instrument, with QTcF > 470 milliseconds; Participants with risk factors for QTcF prolongation, such as uncorrectable hypokalemia, hereditary long QT syndrome; or receiving drugs that prolong QTcF interval (mainly class Ia, Ic, III antiarrhythmic drugs). Drugs with potential to prolong QTcF interval, See Appendix 20.
        2. New York Heart Association (NYHA) Class ≥ 3 congestive heart failure;
        3. Clinically significant arrhythmia, including but not limited to complete left bundle branch block, second degree atrioventricular block;
        4. Known concurrent clinically significant coronary artery disease, cardiomyopathy, severe valvular disease.
        5. Ultrasound Cardiogram performed during the screening showing. Left ventricular ejection fraction LVEF < 50%.
      10. Participants with active bacterial, fungal or viral infections, including active hepatitis B (hepatitis B virus surface antigen positive and hepatitis B virus DNA > 1000 IU/ml or meeting the study site's diagnostic criteria for active hepatitis B infection), hepatitis C (hepatitis C virus RNA positive), or human immunodeficiency virus infection (HIV positive).
      11. Pregnant or lactating women.
      12. Known hypersensitivity to the study drug, other MEK 1/2 inhibitor or its excipients.
      13. Clinically significant condition that, in the opinion of the investigator, would preclude study participation or compliance with safety requirements.
      14. Inability to attend in-person appointments per current clinical site COVID 19 guidelines and restrictions.

Sites / Locations

  • Children's Hospital Los Angeles
  • Principal Investigator Hans
  • John Hopkins All Children Hospital
  • Henry Ford Health System
  • Medical University of South Carolina - Hollings Cancer Center - PPDS
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Research Site
  • Hospital Universitario Vall d'Hebron
  • Hospital Universitario 12 de Octubre
  • Hospital Universitario La Paz

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Single Arm

Arm Description

Outcomes

Primary Outcome Measures

Phase I: Safety: Dose-limiting toxicity (DLT) incidence rate.
Phase I: Safety: MTD and RP2D.
Phase II: Objective response rate (ORR) by BIRC assessment

Secondary Outcome Measures

Phase I Other safety: - The type and frequency of adverse events (AE) - Treatment-Emergent Serious Adverse Events (SAE) - The frequency and causes of death events - Laboratory safety test results - Changes in vital signs
Phase I Changes in NF1-related symptoms.
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Phase I Efficacy: objective response rate (ORR) by investigator /BIRC assessment, clinical benefit rate (CBR) per investigator/BIRC assessment including CR, PR, and SD lasting more than 6 months;
Phase I Clinical outcome variables: patient- and observer-reported outcomes and functional measures
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications, as shown in the table. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Phase I: Maximum Observed Plasma Concentration (Cmax) After Single Dose and Multiple Dose of FCN-159
Phase I: AUC From Time Zero to Last Measurable Concentration (AUClast) After Single Dose and Multiple Dose of FCN-159
Phase I PD marker: ERK phosphorylation inhibition in peripheral blood mononuclear cells (PBMCs)
Phase II: Other efficacy endpoints: Objective Response Rate (ORR)
Proportion of participants with confirmed responsive disease using MRI volumetric analysis
Phase II: Other efficacy endpoints: Clinical Benefit Rate (CBR)
Per investigator/BIRC assessment including CR (Complete Response), PR (Partial Response), and SD (Stable Disease) lasting more than 6 months;
Phase II: Other efficacy endpoints: Disease Control Rate (DCR)
Defined as the percentage of cases with best response (PR or CR or stable disease (SD) after treatment in evaluable cases.
Phase II: Other efficacy endpoints: Progression-Free Survival (PFS)
Defined as the time from participant enrollment to disease progression or death (whichever occurs first). Participants without an event (no progression or death) were censored at the date of last tumor evaluation.
Phase II: Other efficacy endpoints: Time To Progression (TTP)
Defined as the time from participant enrollment to disease progression, and participants without events (without progression or death) were censored at the date of tumor evaluation.
Phase II: Other efficacy endpoints: Time To Response (TTR)
Defined as the time from participant enrollment to the first observation of tumor response among participants with an objective response
Phase II: Other efficacy endpoints: Duration Of Response (DOR)
Defined as the time from first observation of tumor response to tumor progression or death from any cause in participants with an objective response, (whichever occurs first).
Phase II Other safety endpoints: - The type and frequency of adverse events (AE) - Treatment-Emergent Serious Adverse Events (SAE) - The frequency and causes of death events - Laboratory safety test results; - Changes in vital signs;
Phase II Dose intensity
Dose intensity, planned dose intensity and relative dose intensity will be measured. Dose Intensity (mg/day) = Actual Cumulative Dose (mg)/ Total Duration of Exposure (Days). Plan Dose Intensity (mg/day) = Plan Cumulative Dose (mg) / Total Duration of Exposure (Days). Relative Dose Intensity (%) = Dose Intensity / Plan Dose Intensity.
Phase II Changes in NF1-related symptoms
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Phase II Ctrough After Multiple Dose of FCN-159
Phase II Clinical outcome variables: patient- and observer-reported outcomes and functional measures
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications, as shown in the table above. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.

Full Information

First Posted
June 17, 2021
Last Updated
October 16, 2023
Sponsor
Shanghai Fosun Pharmaceutical Industrial Development Co. Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT04954001
Brief Title
Study to Evaluate the Safety, Tolerability, PK Characteristics and Anti-tumor Activity of FCN-159 in Adult and Pediatric Participants With Neurofibromatosis Type 1
Official Title
A Multi-center, Open-label, Single-arm Phase I Dose-escalation and Phase II Dose-expansion Study to Evaluate the Safety, Tolerability, PK Characteristics and Anti-tumor Activity of FCN-159 in Adult and Pediatric Participants With Neurofibromatosis Type 1
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 26, 2021 (Actual)
Primary Completion Date
February 28, 2025 (Anticipated)
Study Completion Date
March 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Fosun Pharmaceutical Industrial Development Co. Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
FCN-159 is a highly active MEK1/2 inhibitor that was designed, synthesized and screened on the basis of the structure of trametinib. FCN-159 is an orally available and highly potent selective inhibitor of MEK1/2, which is expected to be a targeted therapy for the treatment of advanced solid tumors and neurofibromatosis type 1.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurofibromatosis 1, Plexiform Neurofibroma, NF1

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Single Arm
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
FCN-159
Intervention Description
FCN-159 is administered orally in once daily schedule for 28 days a cycle.
Primary Outcome Measure Information:
Title
Phase I: Safety: Dose-limiting toxicity (DLT) incidence rate.
Time Frame
28 days after the dose of FCN-159 for DLT
Title
Phase I: Safety: MTD and RP2D.
Time Frame
Approximately 6-9 months for MTD and RP2D (phase I duration)
Title
Phase II: Objective response rate (ORR) by BIRC assessment
Time Frame
Through study completion, an average of 2 years
Secondary Outcome Measure Information:
Title
Phase I Other safety: - The type and frequency of adverse events (AE) - Treatment-Emergent Serious Adverse Events (SAE) - The frequency and causes of death events - Laboratory safety test results - Changes in vital signs
Time Frame
Through study completion, an average of 2 years
Title
Phase I Changes in NF1-related symptoms.
Description
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Time Frame
Through study completion, an average of 2 years
Title
Phase I Efficacy: objective response rate (ORR) by investigator /BIRC assessment, clinical benefit rate (CBR) per investigator/BIRC assessment including CR, PR, and SD lasting more than 6 months;
Time Frame
Through study completion, an average of 2 years
Title
Phase I Clinical outcome variables: patient- and observer-reported outcomes and functional measures
Description
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications, as shown in the table. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Time Frame
Through study completion, an average of 2 years
Title
Phase I: Maximum Observed Plasma Concentration (Cmax) After Single Dose and Multiple Dose of FCN-159
Time Frame
Pre-dose (0 hour), 0.5, 1, 2, 3, 4, 6, 10, 24 hours post-dose on Cycle 1 Day 1 (1 cycle = 28 days) for single dose, Pre-dose (0 hour), 0.5, 1, 2, 3, 4, 6, 10, 24 hours post-dose on Cycle 1 Day 28 for multiple dose
Title
Phase I: AUC From Time Zero to Last Measurable Concentration (AUClast) After Single Dose and Multiple Dose of FCN-159
Time Frame
Pre-dose (0 hour), 0.5~1, 1.5~3, 4~6, 24 hours on Day 1 of Cycles 2, Pre-dose (0 hour) on Cycle 5 and every 4 cycles thereafter (assessed up to 104 weeks) (1 cycle = 28 days)
Title
Phase I PD marker: ERK phosphorylation inhibition in peripheral blood mononuclear cells (PBMCs)
Time Frame
During Cycle 1 (cycle is 28 days): Day 1, Day 8 and Day 28
Title
Phase II: Other efficacy endpoints: Objective Response Rate (ORR)
Description
Proportion of participants with confirmed responsive disease using MRI volumetric analysis
Time Frame
Through study completion, an average of 2 years
Title
Phase II: Other efficacy endpoints: Clinical Benefit Rate (CBR)
Description
Per investigator/BIRC assessment including CR (Complete Response), PR (Partial Response), and SD (Stable Disease) lasting more than 6 months;
Time Frame
Through study completion, an average of 2 years
Title
Phase II: Other efficacy endpoints: Disease Control Rate (DCR)
Description
Defined as the percentage of cases with best response (PR or CR or stable disease (SD) after treatment in evaluable cases.
Time Frame
Through study completion, an average of 2 years
Title
Phase II: Other efficacy endpoints: Progression-Free Survival (PFS)
Description
Defined as the time from participant enrollment to disease progression or death (whichever occurs first). Participants without an event (no progression or death) were censored at the date of last tumor evaluation.
Time Frame
Through study completion, an average of 2 years
Title
Phase II: Other efficacy endpoints: Time To Progression (TTP)
Description
Defined as the time from participant enrollment to disease progression, and participants without events (without progression or death) were censored at the date of tumor evaluation.
Time Frame
Through study completion, an average of 2 years
Title
Phase II: Other efficacy endpoints: Time To Response (TTR)
Description
Defined as the time from participant enrollment to the first observation of tumor response among participants with an objective response
Time Frame
Through study completion, an average of 2 years
Title
Phase II: Other efficacy endpoints: Duration Of Response (DOR)
Description
Defined as the time from first observation of tumor response to tumor progression or death from any cause in participants with an objective response, (whichever occurs first).
Time Frame
Through study completion, an average of 2 years
Title
Phase II Other safety endpoints: - The type and frequency of adverse events (AE) - Treatment-Emergent Serious Adverse Events (SAE) - The frequency and causes of death events - Laboratory safety test results; - Changes in vital signs;
Time Frame
Through study completion, an average of 2 years
Title
Phase II Dose intensity
Description
Dose intensity, planned dose intensity and relative dose intensity will be measured. Dose Intensity (mg/day) = Actual Cumulative Dose (mg)/ Total Duration of Exposure (Days). Plan Dose Intensity (mg/day) = Plan Cumulative Dose (mg) / Total Duration of Exposure (Days). Relative Dose Intensity (%) = Dose Intensity / Plan Dose Intensity.
Time Frame
Through study completion, an average of 2 years
Title
Phase II Changes in NF1-related symptoms
Description
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Time Frame
Through study completion, an average of 2 years
Title
Phase II Ctrough After Multiple Dose of FCN-159
Time Frame
Pre-dose (0 hour), 0.5~1, 1.5~3, 4~6, 24 hours on Day 1 of Cycles 2, Pre-dose (0 hour) on Cycle 5 and every 4 cycles thereafter (assessed up to 104 weeks) (1 cycle = 28 days)
Title
Phase II Clinical outcome variables: patient- and observer-reported outcomes and functional measures
Description
Each participant will undergo standardized functional evaluations according to the relevant category or categories of PN-related complications, as shown in the table above. The incidence of patients with improved function or quality of life will be measured. Key measurements are chosen from each complication category to assess for change over time.
Time Frame
Through study completion, an average of 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: General inclusion criteria for Phase I and II: 1.Cohort 1: 16-70 years of age (inclusive) with a body weight of ≥ 94 lbs or 42.5 kg. Cohort 2: 2-15 years of age (inclusive) and able to swallow whole tablet. 2.Participants must be diagnosed with NF1-related plexiform neurofibromas (PN) and symptomatic with requirement of systematic therapy per investigator's judgment. A PN is defined as a neurofibroma that has grown along the length of a nerve and may involve multiple fascicles and branches. A spinal PN involves two or more levels with connection between the levels or extending laterally along the nerve. Diagnosis of neurofibromatosis type 1 (NF1) is based on meeting at least 1 of the following 2 diagnostic criteria: Genetic testing confirmation: i.e., positive for NF1 germline mutation per CLIA-certified laboratory (or equivalent) testing. Note: NF1 germline mutation positive must either be confirmed by the FCN-159-002 central laboratory or have documentation of NF1 mutation issued by a CLIA-certified laboratory (or equivalent) - OR - Clinical and imaging confirmation: Meets at least 2 of the following 7 NF1 diagnostic criteria according to the clinical NIH consensus criteria: ≥ 6 cafe-au-lait macules (>0.5 cm in prepubertal participants and > 1.5 cm in post-pubertal participants); Axillary freckling or freckling in inguinal regions; ≥2 neurofibromas of any type, or ≥ 1 plexiform neurofibroma; An optic pathway glioma; ≥2 Lisch nodules (iris hamartomas); A distinctive bony lesion such as dysplasia of the sphenoid bone or dysplasia or thinning of long bone cortex); First-degree relative with NF1. 3. Participants should meet one of the following criteria Must be judged by the investigator to be inoperable for complete resection without causing substantial damage, or unsuitable for surgery with high surgical risks or patient refuses surgery, e.g. due to encasement of or close proximity to vital structures, invasiveness, or high vascularity. NF1 has to cause or has the potential to cause significant morbidity, such as (but not limited to) head and neck lesions that could compromise the airway or great vessels, paraspinal lesions that can cause myelopathy, brachial or lumbar plexus lesions that could cause nerve compression and loss of function, lesions that could result in major deformity (e.g., orbital lesions) or are significantly disfiguring, lesions of the extremity that cause limb hypertrophy or loss of function, and painful lesions. The participants who have previously received surgical treatment, if the PN resection is incomplete, the postoperative residual exceeds 15% of the primary lesion, or relapse after surgery, and the lesions of at least 3 cm are measured in one dimension, are eligible for enrollment. At least a 28-day interval is required between surgery and the first dose of FCN-159. 4. Participants must have a measurable lesion, defined as at least 3 cm in length in at least one dimension, amenable to MRI for efficacy assessment. 5. Adult participants: Karnofsky performance level of ≥70%; Pediatric participants: Lansky performance score ≥ 70%, see Appendix 18. Note: Participants who are wheelchair bound because of paralysis secondary to a plexiform neurofibroma should be considered ambulatory when they are in the wheelchair. Similarly, participants with limited mobility secondary to the need for mechanical support (such as an airway PN requiring tracheostomy or CPAP) will also be considered ambulatory for the purposes of this study. 6. Coagulation function: International normalized ratio (INR) and activated partial thromboplastin time (APTT) ≤ 1.5 ULN. 7. Participants or their legal guardians (if the participant is <18 years old) are able to understand and voluntarily sign a written informed consent form. 8. For participants of childbearing potential: participants must agree to take effective contraception, and receive double barrier contraception, condom, oral or injectable contraceptives, intrauterine device and other contraceptive methods during treatment and for at least 90 days after the last dose. Male participants must agree to avoid sperm donation for at least 90 days after the last dose. 9. Willing to avoid excessive sun exposure and use adequate amounts of sunscreen if sun exposure is anticipated. Exclusion Criteria: Participants who meet any of the following conditions shall not be included in this clinical study: Exclusion criteria for Phase I and II: Participants who have previously received one of the following: Chemotherapy for NF1 within 3 months of enrollment. Ongoing side effects of that treatment > Grade 1 (except alopecia). Treatment with any drug or biologic therapy within 14 days of starting FCN-159, such as: tipifarnib, pirfenidone, Peg-Interferon, sorafenib or other VEGFR inhibitors Strong CYP3A4, CYP2C8 and CYP2C9 inhibitors or inducers (moderate inducers for CYP2C8 and CYP2C9) within 14 days before treatment of the study drug, except for topical skin use. Use of growth factors to increase the number or function of platelets or white blood cells within 7 days before administration of FCN-159. Radiotherapy, surgery or immunotherapy within 4 weeks before administration of FCN-159. Participation in other interventional clinical trials within 4 weeks before administration of FCN-159. Prior treatment with selumetinib or any other MEK 1/2 inhibitors (specific for phase 2 part). Participants with malignant tumors associated with NF1 requiring chemotherapy, radiotherapy, or surgery, such as intermediate- to high-grade optic gliomas or malignant peripheral nerve sheath tumors. Patients have other malignant tumor history or with other malignant tumors simultaneously (excluding cured non-melanoma skin basal cell carcinoma, breast carcinoma in situ or cervix cancer in situ, and other malignant tumors without disease evidence for the past 5 years); Participants who are unable to undergo MRI examination and/or for whom MRI examination is contraindicated (e.g., due to prostheses, orthotics or dental appliances or due to interference with volumetric analysis of target PN on MRI). Uncontrolled hypertension (despite medical therapy) Adult participants: defined as systolic or diastolic blood pressures > 140/90 mmHg on repeat examination with existing anti-hypertension therapy. Pediatric participants: Blood pressure (BP) greater than or equal to the 95th percentile for age, height, and gender measured as described in (Appendix 19). Participants with dysphagia, active digestive diseases, malabsorption syndrome, or other conditions that might affect the absorption of the study drug. Previous or current retinal vein occlusion (RVO), retinal pigment epithelial detachments (RPED), glaucoma and other significant abnormality in ophthalmic examination. Interstitial pneumonia, including existing clinically significant radiation pneumonitis. Cardiac dysfunction or concomitant diseases meeting any one of the following conditions will be excluded: Three 12-lead electrocardiogram (ECG) measurements performed at the study site during the screening period for which the mean value of three measurements was calculated according to the QTcF formula using the instrument, with QTcF > 470 milliseconds; Participants with risk factors for QTcF prolongation, such as uncorrectable hypokalemia, hereditary long QT syndrome; or receiving drugs that prolong QTcF interval (mainly class Ia, Ic, III antiarrhythmic drugs). Drugs with potential to prolong QTcF interval, See Appendix 20. New York Heart Association (NYHA) Class ≥ 3 congestive heart failure; Clinically significant arrhythmia, including but not limited to complete left bundle branch block, second degree atrioventricular block; Known concurrent clinically significant coronary artery disease, cardiomyopathy, severe valvular disease. Ultrasound Cardiogram performed during the screening showing. Left ventricular ejection fraction LVEF < 50%. Participants with active bacterial, fungal or viral infections, including active hepatitis B (hepatitis B virus surface antigen positive and hepatitis B virus DNA > 1000 IU/ml or meeting the study site's diagnostic criteria for active hepatitis B infection), hepatitis C (hepatitis C virus RNA positive), or human immunodeficiency virus infection (HIV positive). Pregnant or lactating women. Known hypersensitivity to the study drug, other MEK 1/2 inhibitor or its excipients. Clinically significant condition that, in the opinion of the investigator, would preclude study participation or compliance with safety requirements. Inability to attend in-person appointments per current clinical site COVID 19 guidelines and restrictions.
Facility Information:
Facility Name
Children's Hospital Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
Principal Investigator Hans
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32608
Country
United States
Facility Name
John Hopkins All Children Hospital
City
Saint Petersburg
State/Province
Florida
ZIP/Postal Code
33701
Country
United States
Facility Name
Henry Ford Health System
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
Facility Name
Medical University of South Carolina - Hollings Cancer Center - PPDS
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
Facility Name
Research Site
City
Beijing
Country
China
Facility Name
Research Site
City
Guangzhou
Country
China
Facility Name
Research Site
City
Hangzhou
Country
China
Facility Name
Research Site
City
Shanghai
Country
China
Facility Name
Research Site
City
Shijiazhuang
Country
China
Facility Name
Research Site
City
Wuhan
Country
China
Facility Name
Hospital Universitario Vall d'Hebron
City
Barcelona
Country
Spain
Facility Name
Hospital Universitario 12 de Octubre
City
Madrid
Country
Spain
Facility Name
Hospital Universitario La Paz
City
Madrid
Country
Spain

12. IPD Sharing Statement

Learn more about this trial

Study to Evaluate the Safety, Tolerability, PK Characteristics and Anti-tumor Activity of FCN-159 in Adult and Pediatric Participants With Neurofibromatosis Type 1

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