Abstract and Schema. Phase 1 and Pharmacokinetic Study of AZD6244 for Recurrent or Refractory Pediatric Low Grade Glioma

Similar documents
Abstract and Schema. Phase 1 and Pharmacokinetic Study of AZD6244 for Recurrent or Refractory Pediatric Low Grade Glioma

Protocol Abstract and Schema

HSV1716 Dose levels and Cohort size Dose level No of Patients HSV1716 Dosage 1* 3 to 6 1 ml of 1 x 10 5 infectious units HSV1716 per ml 2

PBTC-045: Abstract and Schema

Protocol Abstract and Schema

Protocol Abstract and Schema

Feasibility Trial of Optune for Children with Recurrent or Progressive Supratentorial High-Grade Glioma and Ependymoma

Protocol Abstract and Schema

Protocol Abstract and Schema

Protocol Abstract and Schema

Randomized Phase II Study of Irinotecan and Cetuximab with or without Vemurafenib in BRAF Mutant Metastatic Colorectal Cancer

BR for previously untreated or relapsed CLL

CombiRT in Metastatic Melanoma Trial

Synopsis. Study Phase and Title: Study Objectives: Overall Study Design

COG-ACNS1123: Phase 2 Trial of Response-Based Radiation Therapy for Patients with Localized Central Nervous System Germ Cell Tumors (CNS GCT)

FAST FACTS Eligibility Reviewed and Verified By MD/DO/RN/LPN/CRA Date MD/DO/RN/LPN/CRA Date Consent Version Dated

Aquila Smoldering Multiple Myeloma

FAST FACTS Eligibility Reviewed and Verified By MD/DO/RN/LPN/CRA Date MD/DO/RN/LPN/CRA Date Consent Version Dated

Figure 1: PALLAS Study Schema. Endocrine adjuvant therapy may have started before randomization and be ongoing at that time.

Cancer Research Group Version Date: November 5, 2015 NCI Update Date: January 15, Schema. L O Step 1 1,2

Accrual Status We are currently only enrolling patients who are either:

Ana Luisa Stuckett, PhD, MS

Plattenepithelkarzinom des Ösophagus, 1 st -line

Alliance A Symptomatic brain radionecrosis after receiving radiosurgery for

CHK1 Inhibitor. Prexasertib, LY MsOH H 2 O. Drug Discovery Platform: Cancer Cell Signaling

FAST FACTS Eligibility Reviewed and Verified By MD/DO/RN/LPN/CRA Date MD/DO/RN/LPN/CRA Date Consent Version Dated

COG-ACNS1422: A Phase 2 Study of Reduced Therapy for Newly Diagnosed Average-Risk WNT-Driven Medulloblastoma Patients

Primary Endpoint The primary endpoint is overall survival, measured as the time in weeks from randomization to date of death due to any cause.

Panobinostat, Bortezomib and Dexamethasone

FAST FACTS Eligibility Reviewed and Verified By MD/DO/RN/LPN/CRA Date MD/DO/RN/LPN/CRA Date Consent Version Dated

BC Cancer Protocol Summary for Maintenance Therapy of Multiple Myeloma Using Lenalidomide

Appendix ZOOM Etude pour site internet

Supplementary Appendix

NP30179 Eligibility Screening Form (ESF) Version 3.0

Panitumumab After Resection of Liver Metastases From Colorectal Cancer in KRAS Wild-type Patients

PankoMab-GEX Versus Placebo as Maintenance Therapy in Advanced Ovarian Cancer

UMN request : information to be made public Page 1

Supplementary Appendix

Subject ID: I N D # # U A * Consent Date: Day Month Year

Cancer Research Group Version Date: June 22, 2016 NCI Update Date: November 13, Schema

Alliance A Phase II Tri al Of SMO/AKT/NF2 Inhi bi tors In Progressi ve Meni ngi omas Wi th SMO/AKT/ NF2 Mutati ons

Kymriah. Kymriah (tisagenlecleucel) Description

NCCP Chemotherapy Regimen. Carfilzomib, Lenalidomide and Dexamethasone (KRd) Therapy - 28 day

Low-dose AZA, Pioglitazone, ATRA Versus Standard-dose AZA in Patients >=60 Years With Refractory AML (AML-ViVA)

CNAJ12TZRT. Protocol Code. Neuro-Oncology. Tumour Group. Dr. Brian Thiessen. Contact Physician

BCCA Protocol Summary for Therapy of Relapsed Multiple Myeloma Using Lenalidomide with Dexamethasone

MM relaps efter min. 3 linie behandlinger.

Arm A: Induction Gemcitabine 1000 mg/m 2 IV once a week for 6 weeks.

CHMP Type II variation assessment report

Crizotinib in addition to Radiotherapy and TMZ in newly diagnosed GBM

PDF of Trial CTRI Website URL -

Selumetinib (AZD6244; ARRY ) Pediatric MATCH. George Kirk June 2016

BC Cancer Protocol Summary for Therapy of Acute Myeloid Leukemia Using azacitidine and SORAfenib

DESIGN DE L ETUDE Environ 406 patients seront randomisés dans l un des 3 bras de l étude selon le schéma cidessous

Cisplatin Vinorelbine (Oral) therapy +/- radiotherapy

Clinical Study Synopsis

(7) VITAL SIGNS (8) LEVEL OF CONSCIOUSNESS (9) MENTAL STATUS (10) SPEECH (11) VISION (12) FUNDUS (PAPILLEDEMA)

NCCP Chemotherapy Regimen. Olaparib Monotherapy

Patients must have met all of the following inclusion criteria to be eligible for participation in this study.

* Dose may vary dependent on tolerability and co-morbidities

Keeping track of your numbers

Doxorubicin and Ifosfamide Sarcoma

SUBCUTANEOUS Bortezomib + Thalidomide +Dexamethasone Available for Routine Use in

Bortezomib, Thalidomide and Dexamethasone (VTD) 28 day

LONSURF (trifluridine-tipiracil) oral tablet

ALK Inhibition: From Biology to Approved Therapy for Advanced Non-Small Cell Lung Cancer

Carfilzomib and Dexamethasone (CarDex)

Cisplatin Doxorubicin Sarcoma

In- and exclusion criteria

ELIGIBILITY: Newly diagnosed acute promyelocytic leukemia (APL) with high risk (WBC more than 10 x 10 9 /L)

2. Is therapy prescribed by, or in consultation with, a hematologist and/or oncologist?

Clinical Trial Results Database Page 1

BCCA Protocol Summary for Therapy of Multiple Myeloma Using Pomalidomide with Dexamethasone

screening procedures Disease resistant to full-dose imatinib ( 600 mg/day) or intolerant to any dose of imatinib

ASCT After a Rituximab/Ibrutinib/Ara-c Containing induction in Generalized Mantle Cell Lymphoma

June Schema: S T R A I T I F Y. Age 1. <50 2. >50

Trial record 1 of 1 for: Previous Study Return to List Next Study

A pediatric phase 1 study of larotrectinib, a highly selective inhibitor of the tropomyosin receptor kinase (TRK) family: an updated analysis

BC Cancer Protocol Summary for Treatment of Elderly Newly Diagnosed Glioma Patient with Concurrent and Adjuvant Temozolomide and Radiation Therapy

Lung Pathway Group Cisplatin & PO Vinorelbine in Non- Small Cell Lung Cancer (NSCLC)

WARNING, CONTRAINDICATIONS, WARNINGS AND PRECAUTIONS,

BC Cancer Protocol Summary for Therapy of Multiple Myeloma Using Carfilzomib, Lenalidomide with Dexamethasone

LYNPARZA (olaparib) oral capsule and tablet

TKIs ( Tyrosine Kinase Inhibitors ) Mechanism of action and toxicity in CML Patients. Moustafa Sameer Hematology Medical Advsior,Novartis oncology

NEXAVAR (sorafenib tosylate) oral tablet

ULYRICE. Protocol Code. Lymphoma. Tumour Group. Dr. Laurie Sehn. Contact Physician

UMN request : information to be made public Page 1

June 2009 Breast Committee CALGB 40502

Efficacy and Safety of the Combination Therapy of Dabrafenib and Trametinib in Subjects With BRAF V600E- Mutated Rare Cancers

Study Rationale. Reference: Chanan-Khan, A., et al., ASH 2010, Abstract#1962. Reference: Whiteman, K., et al, AACR, 2009, Abstract#2799

Vincristine Ifosfamide Doxorubicin Etoposide (VIDE) Sarcoma

Rituximab, Gemcitabine, Dexamethasone and Cisplatin RGDP Regimen

STARTING PATIENTS ON. AA-CLOZAPINE is the only Canadian-made treatment indicated for the symptoms of treatment-resistant schizophrenia.

Cisplatin100 plus Radiotherapy for locally Advanced Squamous Cell Carcinoma Head and Neck

A Phase I Dose Escalation Study of Intratumoral Herpes Simplex Virus 1 Mutant rrp450 in Patients with Refractory Sarcoma or Neuroblastoma

Xalkori. Xalkori (crizotinib) Description

WT1 peptide cancer vaccine for solid tumors Phase I/II Clinical Trials Registration Form

Gemcitabine & Cisplatin

PRINCESS MARGARET CANCER CENTRE CLINICAL PRACTICE GUIDELINES

R-GDP: Rituximab, Gemcitabine, Dexamethasone &Cisplatin

Transcription:

Abstract and Schema Phase 1 and Pharmacokinetic Study of AZD6244 for Recurrent or Refractory Pediatric Low Grade Glioma Description and Rationale: Low grade gliomas are among the most common primary CNS neoplasms of childhood. Recent studies demonstrate constitutive activation of the BRAF oncogene by multiple mechanisms. The most common mechanism observed is a genetic fusion which results in loss of the regulatory domain of BRAF; this fusion gene is described in the majority of JPA specimens examined. Alternate mechanisms of activation, such as the BRAF V600E mutation have also been described in low grade glioma. BRAF is a component of the Ras/Raf/MAP kinase signaling cascade, and constitutive activation of BRAF results in increased MAP kinase signaling, with subsequent cellular proliferation. We propose that inhibition of the MAP kinase MEK1 and 2 will have antitumor effects in BRAF activated tumors. AZD6244 is an orally available small molecule inhibitor of the MAP kinase MEK1 and 2. Preclinical studies demonstrate that it results in MEK1and 2 inhibition (measured by ERK1 and 2 phosphorylation). An initial Phase 1 study in adult patients also suggests that treatment with AZD6244 inhibits ERK phosphorylation in PBMC and in post treatment tumor specimens at tolerable doses. This is a multicenter, phase 1 and pharmacokinetic trial to determine the MTD and/or select a recommended phase 2 dose of AZD6244 in children 12 years or over with recurrent or refractory low grade glioma following radiation and/or chemotherapy. Schema: This is a dose escalation trial of AZD6244 administered orally twice daily for 28 consecutive days. Courses will be repeated every 28 days and continue for 13 courses or until one of the Offtreatment criteria have been met. The starting dose for patients is 33mg/m 2 /dose, BID for a total daily dose of 66mg/m 2 /day. Dose escalations will be performed according to the Table below until the MTD or the recommended phase two dose (RP2D) is identified. Table 2 Dose Level Dose 0 25 mg/m 2 /dose, BID (total daily dose 50 mg/m 2 /day) 1* 33 mg/m 2 /dose, BID (total daily dose 66 mg/m 2 /day) 2 43 mg/m 2 /dose, BID (total daily dose 86 mg/m 2 /day) 3 56 mg/m 2 /dose, BID (total daily dose 112 mg/m 2 /day) 4 73mg/m 2 /dose, BID (total daily dose 146 mg/m 2 /day) 5 95 mg/m 2 /dose, BID (total daily dose 190 mg/m 2 /day) *Starting dose level. Page 1 of 6

1.1 Primary Objectives 1.1.1 To estimate the maximum tolerated dose (MTD) or recommend a Phase II dose of AZD6244 in children with recurrent or refractory low-grade glioma. 1.1.2 To describe the toxicity profile and define the dose limiting toxicity of AZD6244 in children with recurrent or refractory low-grade glioma. 1.1.3 To study the safety of the maximum tolerated dose (MTD) or recommended a Phase II dose (RP2D) of AZD6244 as determined based on safety data from children 12 years of age in children <12 years of age. If the MTD/RP2D of the older children is too toxic for the younger children, we will de-escalate to one dose level below and study the safety of that dose in the younger age cohort. 1.1.4 To characterize the inter- and intra-patient variability in AZD6244 pharmacokinetics administered on this schedule in patients <12 years of age at the MTD/RP2D. 1.2 Secondary Objectives 1.2.1 To characterize the inter- and intra-patient variability in AZD6244 pharmacokinetics administered on this schedule and to assess the influence of patient specific covariates (including concomitant drug therapy) on AZD6244 pharmacokinetics. 1.2.2 To evaluate the feasibility of collecting pre-trial tumor samples and the feasibility of using immunohistochemical assays to identify BRAF aberrations in available tumor specimens. 1.2.3 To determine if pre-trial tumor samples show the biochemical signature that indicates activation of the MAPK pathway. 1.2.4 To describe MRI characteristics of the tumors before and after treatment and to explore the diffusion changes in the tumors before and after treatment to determine if there is an early diffusion indicator of response. 1.2.5 Within the constraints of a Phase I trial, to document antitumor activity of treatment with AZD6244, as measured by objective responses and PFS. 1.2.6 To explore the pharmacogenetic polymorphisms in AZD6244 metabolizing enzymes and transporters and relate these polymorphisms to AZD6244 pharmacokinetics. 2 PATIENT SELECTION Eligibility Assessment Timelines Imaging evaluations necessary to establish eligibility for study entry must be done within three (3) weeks prior to registration. All other evaluations necessary to establish eligibility for study entry must be done within two (2) weeks prior to registration. Criteria to Start Treatment Patients must start therapy within 7 working days of registration. Page 2 of 6

Laboratory values must be no older than seven(7) days prior to the start of therapy. If a test that is repeated after registration and prior to therapy is outside the limits for eligibility, it must be rechecked 48 hours prior to the start of therapy. If the recheck is still outside the limits for eligibility, the patient may not receive protocol therapy. All patients must meet the following inclusion and exclusion criteria. NO EXCEPTIONS WILL BE GIVEN. 2.1 Eligibility Criteria 2.1.1 Tumor Patients with a histologically confirmed diagnosis of low grade gliomas (WHO Grades I & II) that is recurrent or refractory. Patients with optic pathway gliomas are eligible with clinical and/or radiographic evidence of progression. 2.1.2 Prior Therapy Patients must have received prior therapy other than surgery and must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to entering this study. 2.1.2.1 Myelosuppressive chemotherapy: Patients must have received their last dose of known myelosuppressive anticancer chemotherapy at least three weeks prior to study registration or at least six weeks if nitrosourea. 2.1.2.2 Biologic agent: Patient must have recovered from any acute toxicity potentially related to the agent and received their last dose of the biologic agent 7 days prior to study registration. For biologic agents that have a prolonged half-life, at least three half-lives must have elapsed prior to registration 2.1.2.3 Monoclonal antibody treatment: At least three half-lives must have elapsed prior to registration. Note: A list of the half-lives of commonly used monoclonal antibodies is available on the PBTC webpage under Generic Forms and Templates. 2.1.2.4 Radiation: Patients must have: o Had their last fraction of local irradiation to primary tumor 12 weeks prior to registration; investigators are reminded to review potentially eligible cases to avoid confusion with pseudo-progression. o Had their last fraction of craniospinal irradiation (>24Gy) or total body irradiation > 3 months prior to registration 2.1.2.5 Bone Marrow Transplant: Patient must be: o 6 months since allogeneic bone marrow transplant prior to registration o 3 months since autologous bone marrow/stem cell prior to registration Page 3 of 6

2.1.2.6 Corticosteroids: Patients who are receiving dexamethasone must be on a stable or decreasing dose for at least 1 week prior to registration. 2.1.2.7 Growth factors Off all colony forming growth factor(s) for at least 1 week prior to registration (filgrastim, sargramostim, erythropoietin) and at least 2 weeks for longacting formulations. 2.1.3 Age Patient must be 3 but 21 years of age at registration. 2.1.4 BSA Patients treated at 25mg/m 2 /dose BID must have BSA 0.55m 2. 2.1.5 Neurological Status Patients with neurological deficits should have deficits that are stable for a minimum of 1 week prior to registration. 2.1.5.1 Patients must be able to swallow capsules 2.1.6 Performance Status Karnofsky Performance Scale (KPS for > 16 yrs of age) or Lansky Performance Score (LPS for 16 years of age) 60 assessed within two weeks prior to registration. 2.1.7 Organ Function Patients must have normal organ and marrow function documented within 14 days of registration and within 7 days of the start of treatment as noted below: Absolute neutrophil count >1,000/µL (unsupported) Platelets >100,000/µL (unsupported) Hemoglobin 8 g/dl (may be supported) Total bilirubin < 1.5 times upper limit of normal for age AST(SGOT)/ALT(SGPT) <2.5 X institutional upper limit of normal for age Creatinine clearance or radioisotope GFR 70 ml/min/1.73m 2 or a serum creatinine based on age as follows: Table 1 Age (years) 5 0.8 > 5 but 10 1 >10 but 15 1.2 >15 1.5 Maximum Serum Creatinine (mg/dl) Sodium, Potassium, Calcium and Magnesium within the institutional limits of normal Albumin 3 g/dl 2.1.8 Pregnancy Status Female patients of childbearing potential must not be pregnant or breast-feeding. Female patients of childbearing potential must have a negative serum or urine pregnancy test. Page 4 of 6

2.1.9 Pregnancy Prevention The effects of AZD6244 on the developing human fetus are unknown. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation, and for four weeks after dosing with AZD6244 ceases. Women of child-bearing potential must have a negative pregnancy test prior to entry. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. Please note that the AZD6244 manufacturer recommends that adequate contraception for male patients should be used for 16 weeks post-last dose due to sperm life cycle. 2.1.10 Informed Consent Ability to understand and the willingness to sign a written informed consent document according to institutional guidelines. 2.2 Exclusion Criteria 2.2.1 Patients with any clinically significant unrelated systemic illness (serious infections or significant cardiac, pulmonary, hepatic or other organ dysfunction), likely interfere with the study procedures or results. 2.2.2 Patients who are receiving any other anticancer or investigational agents. 2.2.3 Patients with uncontrolled seizures are not eligible for the study. 2.2.4 Previous MEK inhibitor use such as PD-0325901; CI1040; AS73026; GDC 0973; ARRY43182; GSK110212. 2.2.5 Prior treatment with a BRAF inhibitor 2.2.6 History of allergic reactions attributed to compounds of similar chemical or biologic composition to AZD6244. 2.2.7 Patients with QTc interval >450 msecs or other factors that increase the risk of QT prolongation or arrhythmic events (e.g., heart failure, hypokalemia, family history of long QT interval syndrome) including heart failure that meets New York Heart Association (NYHA) class III and IV definitions are excluded. 2.2.8 Required use of a concomitant medication that can prolong the QT interval. 2.2.9 History of allergic reactions attributed to compounds of similar chemical or biologic composition to AZD6244. 2.3 Inclusion of Women and Minorities Both men and women of all races and ethnic groups are eligible for this trial. Page 5 of 6

2.4 Other All patients must have current and past smoking status recorded in the PedBraTum database. 2.5 Treatment at Primary Institution All experimental protocol therapy should be administered/ dispensed and all imaging studies obtained at the primary institution. Laboratory studies, excluding pharmacokinetic and biologic assays, may be performed at a CLIA certified laboratory of the investigator s choice. Page 6 of 6