NANT 2015-02: A Phase 1 Study of Lorlatinib (PF-06463922)

Phase 1

Active, not recruiting

• Conditions: Neuroblastoma
• Interventions: Drug: Lorlatinib; Drug: Cyclophosphamide; Drug: Topotecan; Drug: Filgrastim/pegfilgrastim

• Registration Number: NCT03107988
• Lead Sponsor: New Approaches to Neuroblastoma Therapy Consortium

Brief Summary

Lorlatinib is a novel inhibitor across ALK variants, including those resistant to crizotinib. In this first pediatric phase 1 trial of lorlatinib, the drug will be utilized as a single agent and in combination with chemotherapy in patients with relapsed/refractory neuroblastoma. The dose escalation phase of this study (Cohort A1) uses a traditional Phase I 3+3 design. Once a recommended phase 2 pediatric dose is identified, an expansion cohort of 6 patients (Cohort B1), within which ALKi naïve patients will be prioritized, will be initiated. Parallel cohorts will be initiated in adults or patients with large BSA (Cohort A2) and in combination with chemotherapy upon establishing RP2D (Cohort B2).

Detailed Description

Lorlatinib is a novel inhibitor across ALK variants, including those resistant to crizotinib. An adult phase 1 study established an RP2D of 100mg QD for lorlatinib. In this first pediatric phase 1 trial of lorlatinib, the drug will be utilized as a single agent and in combination with chemotherapy in patients with relapsed/refractory neuroblastoma. The dose escalation phase of this study (Cohort A1) uses a traditional Phase I 3+3 design. Once a recommended phase 2 pediatric dose is identified, an expansion cohort of 6 patients (Cohort B1), within which ALKi naïve patients will be prioritized, will be initiated. Parallel cohorts will be initiated in adults or patients with large BSA (Cohort A2) and in combination with chemotherapy upon establishing RP2D (Cohort B2).

Lorlatinib will be administered orally via tablets or via oral dispersion if patient is unable to swallow tablets whole

All patients will participate in mandatory pharmacokinetic testing.

Study Timeline

• Study First Submitted: 2017-03-21
• Study First Submitted QC: 2017-04-04
• Study First Posted: 2017-04-11
• Study Start: 2017-09-05
• Status Verified: 2025-02
• Last Update Submitted: 2025-05-06
• Last Update Posted: 2025-05-11
• Primary Completion: 2025-12
• Study Completion: 2025-12

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 65

Inclusion Criteria

1. Patients are required to have an activating ALK aberration in their tumor detected by certified assay (i.e. CLIA in the US.) prior to registration. The report from this test is required to be submitted for eligibility. Patients with at least one of the following genetic features in their tumor will be considered to have an activating ALK aberration:

1. An ALK activating mutation; 2. ALK amplification (> 10 signals of the ALK gene); 3. Presence of any ALK fusion protein that arises from a chromosomal translocation 2) Patients must have a diagnosis of neuroblastoma either by histologic verification of neuroblastoma and/or demonstration of tumor cells in the bone marrow with increased urinary catecholamines.

3. Patients must have a history of high-risk neuroblastoma according to COG risk classification at the time of study registration. Patients who were initially considered low or intermediate-risk, but then reclassified as high-risk are also eligible.

4. All patients must have at least one of the following

a) Recurrent/progressive disease: after the diagnosis of high risk neuroblastoma at any time prior to enrollment regardless of response to frontline therapy b) No prior history of recurrent/progressive disease since the diagnosis of high risk neuroblastoma b1) Refractory disease- a best overall response of no response/stable disease since diagnosis of high risk neuroblastoma and at least 4 cycles of induction therapy. No prior history of recurrent/progressive disease since the diagnosis of high risk neuroblastoma.

b2) Persistent disease- a best overall response of no partial response since diagnosis of high risk neuroblastoma and at least 4 cycles of induction therapy. No prior history of recurrent/progressive disease since the diagnosis of high risk neuroblastoma.

5. Patients must have at least ONE of the following (lesions may have received prior radiation therapy as long as they meet the other criteria listed below):

1. For recurrent/progressive or refractory disease, at least one MIBG avid bone site.

2. For persistent disease, if a patient has 3 or more MIBG avid lesions, then no biopsy is required. If a patients has only 1 or 2 MIBG avid bone lesion sites then biopsy confirmation of neuroblastoma or ganglioneuroblastoma in at least one MIBG avid site present at the time of enrollment is required to be obtained at any time point prior to enrollment.

3. For MIBG non-avid tumors, patients must have at least one FDG avid site and a biopsy confirmation of neuroblastoma and/or ganglioneuroblastoma at any time prior to enrollment from at least one FDG-avid site.

   6. Any amount of neuroblastoma tumor cells in the bone marrow done at the time of study enrollment based on routine morphology with or without immunocytochemistry in at least one sample from bilateral aspirates and biopsies.

   7. At least one soft tissue lesion that meets criteria for a TARGET lesion as defined by:

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1. SIZE: Lesion can be accurately measured in at least one dimension with a longest diameter ≥ 10 mm, or for lymph nodes ≥ 15 mm on short axis. Lesions meeting size criteria will be considered measurable.

2. In addition to size, a lesion needs to meet one of the following criteria except for patients with parenchymal CNS lesions which only need to meet size criteria:

   b1) MIBG avid. For patients with recurrent/progressive or refractory disease, no biopsy is required. For patients with persistent disease only: If a patient has only 1 or 2 MIBG avid lesions sites, then biopsy confirmation of neuroblastoma and/or ganglioneuroblastoma in at least one MIBG avid site present at time of enrollment is required to be obtained. If a patient has 3 or more MIBG avid lesions, then no biopsy is required.

   b2) MIBG non avid tumors: Patients must have at least one FDG avid site and biopsy confirmation of neuroblastoma and/or ganglioneuroblastoma in at least one FDG-PET avid site present at the time of enrollment.

   8. At least one non-target soft tissue lesion that is not measurable, but had a biopsy positive for neuroblastoma and/or ganglioneuroblastoma or is MIBG avid at any time prior to enrollment.

   9. Patients must have a life expectancy of at least 12 weeks and a Lansky (≤16 years) or Karnofsky (>16 years) score of at least 50.

   10. Prior Therapy

   1. Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to study registration.

   2. Patients must not have received the therapies indicated below after disease evaluation or within the specified time period prior to registration on this study as follows:

   3. Myelosuppressive chemotherapy: must not have received within 2 weeks prior to registration.

   4. Biologic anti-neoplastics- agents not known to be associated with reduced platelet or ANC counts (including retinoids): must not have received within 7 days prior to registration.

   5. Monoclonal antibodies: must have received last dose at least 7 days or 3 half-lives whichever is longer, but no longer than 30 days (with recovery of any associated toxicities), prior to protocol therapy.

   6. Cellular Therapy (e.g. modified T cells, NK cells, dentritic cells etc.): must not have received within 3 weeks and resolution of all toxicities.

   7. Radiation: must not have received small port radiation within 7 days prior to registration.

   8. Hematopoietic Stem Cell Transplant: 7. IVIG 11) All patients must have adequate organ function defined as:

   • Hematological Function:

   1. Absolute Phagocyte count (APC= neutrophils and monocytes): ≥ 1000/µL

   2. Absolute Neutrophil count: ≥750/µL

   3. Absolute Lymphocyte count ≥ 500/µL

   4. Platelet count: ≥ 50,000/µL (A1, A2, and B1); ≥ 75,000/µL (B2), transfusion independent (no platelet transfusions within 1 week)

   5. Hemoglobin ≥ 10 g/dL (may transfuse)

   6. Patients with known bone marrow metastatic disease will be eligible for study as long as they meet hematologic function criteria above.

   • Renal Function: Age-adjusted serum creatinine ≤ to 1.5 x normal for age/gender OR creatinine clearance or GFR greater than or equal to 60 cc/min/1.73m2

   • Liver Function: Total bilirubin ≤ 1.5 x normal for age, AND SGPT (ALT) 135 and SGOT (AST) ≤ 3 x upper limit of normal. Sinusoidal obstruction syndrome (SOS) if present, must be stable or improving clinically

   • Cardiac Function: Normal ejection fraction documented by either echocardiogram or radionuclide MUGA evaluation OR Normal fractional shortening documented by echocardiogram

   • Pulmonary Function: No dyspnea at rest, no oxygen requirement.

   • Neuropsychological Function: Patients must exhibit ≤ grade 1 as defined by CTCAE V4 of nervous system disorders and psychiatric disorders 12) Reproductive Status: All post-menarchal females must have a negative beta-HCG. Males and females of reproductive age and childbearing potential must use effective contraception for the duration of their participation.

     13. Patients with other ongoing serious medical issues must be approved by the study chair prior to registration.

     14. Prior ALK inhibitor treatment- patients must not have been previously treated with lorlatinib. Prior therapy with other ALK inhibitors is allowed.

     15. Concomitant Therapy Restrictions:

     1. Patients may not receive any other anti-cancer agents or radiotherapy while on protocol therapy.
     2. Patient must not be receiving chronic systemic corticosteroids at doses greater than physiologic dosing (inhaled corticosteroids acceptable)
     3. CYP34A inhibitors
     4. CYP34A inducers
     5. CYP34A substrates

Exclusion Criteria

• Pregnancy, breast feeding, or unwillingness to use effective contraception during the study.
  • Patients who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study.
  • Patients with disease of any major organ system that would compromise their ability to withstand therapy.
  • Patients who have received prior allogeneic stem cell transplant
  • Patients who are on hemodialysis.
  • Patients with an active or uncontrolled infection.
  • Known history of human immunodeficiency virus (HIV) infection, hepatitis B, or hepatitis C.
  • Patient with known history of acute or chronic severe psychiatric disorders
  • Patient with current history of suicidal ideation and history of suicide attempt in their lifetime
  • Patient declines participation in NANT 2004-05, the NANT Biology Study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cohort A1 DL1	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days. The dose level of lorlatinib will be 45 mg/m2/dose. Patients must be under 18 years of age at time of enrollment.
Cohort A2 3A	Lorlatinib	Lorlatinib will be given at 100 mg orally once daily continuously for 28 days. Patients must be 18 years of age or older at time of enrollment.
Cohort B1	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days at the RP2D defined by cohort A1 (115mg/m2/dose). This cohort will not begin enrollment until the recommended phase 2 dose is established from the dose escalation cohort A1. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL4B	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days at 95mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL4B	Filgrastim/pegfilgrastim	Lorlatinib will be given orally once daily continuously for 28 days at 95mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL4B	Cyclophosphamide	Lorlatinib will be given orally once daily continuously for 28 days at 95mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL4B	Topotecan	Lorlatinib will be given orally once daily continuously for 28 days at 95mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort A1 DL2	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days. The dose level of lorlatinib will be 60 mg/m2/dose. Patients must be under 18 years of age at time of enrollment.
Cohort A1 DL3	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days. The dose level of lorlatinib will be 75 mg/m2/dose. Patients must be under 18 years of age at time of enrollment.
Cohort A1 DL4	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days. The dose level of lorlatinib will be 95 mg/m2/dose. Patients must be under 18 years of age at time of enrollment.
Cohort A1 DL5	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days. The dose level of lorlatinib will be 115 mg/m2/dose. Patients must be under 18 years of age at time of enrollment.
Cohort A2 4A	Lorlatinib	Lorlatinib will be given at 150 mg orally once daily continuously for 28 days. Patients must be 18 years of age or older at time of enrollment.
Cohort A2 Expansion 4A	Lorlatinib	Lorlatinib will be given at 150 mg orally once daily continuously for 28 days. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL5B	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days at 115mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL5B	Cyclophosphamide	Lorlatinib will be given orally once daily continuously for 28 days at 115mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL5B	Topotecan	Lorlatinib will be given orally once daily continuously for 28 days at 115mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL5B	Filgrastim/pegfilgrastim	Lorlatinib will be given orally once daily continuously for 28 days at 115mg/m2/dose. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be under 18 years of age at time of enrollment.
Cohort B2 DL3A	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days at 100mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL3A	Cyclophosphamide	Lorlatinib will be given orally once daily continuously for 28 days at 100mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL3A	Topotecan	Lorlatinib will be given orally once daily continuously for 28 days at 100mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL3A	Filgrastim/pegfilgrastim	Lorlatinib will be given orally once daily continuously for 28 days at 100mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL4A	Lorlatinib	Lorlatinib will be given orally once daily continuously for 28 days at 150mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL4A	Cyclophosphamide	Lorlatinib will be given orally once daily continuously for 28 days at 150mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL4A	Topotecan	Lorlatinib will be given orally once daily continuously for 28 days at 150mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.
Cohort B2 DL4A	Filgrastim/pegfilgrastim	Lorlatinib will be given orally once daily continuously for 28 days at 150mg/day. Lorlatinib should be administered at least one hour prior to conventional chemotherapy (Cyclophosphamide and Topotecan) on days 1-5 of each cycle. Patients must be 18 years of age or older at time of enrollment.

Primary Outcome Measures

Name	Time	Method
MTD/RP2D determination A1	All toxicities from enrollment until completion of course 2 (Day 56)	Proportion of patients with course 1 DLT and/or course 2 neuropsychological DLT in cohort A1
MTD/RP2D determination A2	All toxicities from enrollment until completion of course 2 (Day 56)	Proportion of patients with course 1 DLT and/or course 2 neuropsychological DLT in cohort A2
MTD/RP2D determination B2	All toxicities from enrollment until completion of course 1 (Day 28)	Proportion of patients with course 1 DLT in cohort B2
Describe Hematological Toxicities (A2)	All toxicities from enrollment through 30 days following end of protocol therapy	Proportion of patients with any grade 3 or greater hematological toxicities in A2
Describe Non-Hematological Toxicities (A1 and B1)	All toxicities from enrollment through 30 days following end of protocol therapy	Proportion of patients with any grade 3 or greater non-hematological toxicities on any course in A1 and B1
Describe Hematological Toxicities (A1 and B1)	All toxicities from enrollment through 30 days following end of protocol therapy	Proportion of patients with any grade 3 or greater hematological toxicities on any course in A1 and B1
Describe Non-Hematological Toxicities (B2)	All toxicities from enrollment through 30 days following end of protocol therapy	Proportion of patients with any grade 3 or greater non-hematological toxicities in B2
Describe Hematological Toxicities (B2)	All toxicities from enrollment through 30 days following end of protocol therapy	Proportion of patients with any grade 3 or greater hematological toxicities in B2
Describe Non-Hematological Toxicities (A2)	All toxicities from enrollment through 30 days following end of protocol therapy	Proportion of patients with any grade 3 or greater non-hematological toxicities in A2

Secondary Outcome Measures

Name	Time	Method
Pharmacokinetics B2	Day 1 through Day 15	Steady State AUC and Cmax for lorlatinib in patients in cohort B2
Overall Response B2	From Day 1 of protocol therapy through 30 days following end of protocol therapy	Proportion of patients evaluable for response with a best overall response of CR/CR-MD/PR for patients in cohort B2
Pharmacokinetics A1 and B1	Day 1 through Day 15	Steady State AUC and Cmax for lorlatinib in patients in cohort A1 and B1
Pharmacokinetics A2	Day 1 through Day 15	Steady State AUC and Cmax for lorlatinib in patients in cohort A2
Overall Response A1 and B1	From Day 1 of protocol therapy through 30 days following end of protocol therapy	Proportion of patients evaluable for response with a best overall response of CR/CR-MD/PR for patients in cohort A1 and B1
Overall Response A2	From Day 1 of protocol therapy through 30 days following end of protocol therapy	Proportion of patients evaluable for response with a best overall response of CR/CR-MD/PR for patients in cohort A2

Trial Locations

Locations (13)

Royal Marsden Hospital; 🇬🇧 Sutton, Surrey, United Kingdom

Cook Children's Healthcare System; 🇺🇸 Fort Worth, Texas, United States

Children's Healthcare of Atlanta; 🇺🇸 Atlanta, Georgia, United States

Children's Hospital Los Angeles; 🇺🇸 Los Angeles, California, United States

Children Hospital of Colorado; 🇺🇸 Aurora, Colorado, United States

UCSF Helen Diller Family Comprehensive Cancer Center; 🇺🇸 San Francisco, California, United States

Children's Hospital of Philadelphia; 🇺🇸 Philadelphia, Pennsylvania, United States

University of Chicago, Comer Children's Hospital; 🇺🇸 Chicago, Illinois, United States

Childrens Hospital Boston, Dana-Farber Cancer Institute.; 🇺🇸 Boston, Massachusetts, United States

C.S Mott Children's Hospital; 🇺🇸 Ann Arbor, Michigan, United States

Children's Hospital and Regional Medical Center - Seattle; 🇺🇸 Seattle, Washington, United States

Hospital for Sick Children; 🇨🇦 Toronto, Ontario, Canada

Institut Curie; 🇫🇷 Paris, Cedex, France