Alisertib and TAK-228 in Participants With Human Papilloma Virus (HPV) Associated Malignancies

NCT02812056 | Withdrawn Phase 1

• 2 other identifiers: 2015-0689NCI-2016-01190
• Study Type: interventional
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

The goal of this clinical research study is to find the highest tolerable dose of the combination of alisertib and TAK-228 that can be given to participants with advanced solid tumors that are associated with HPV. Researchers also want to learn if the study drug combination can help to control advanced solid tumors.

Conditions

Malignant Neoplasms of Digestive Organs; Malignant Neoplasms of Female Genital Organs; Malignant Neoplasms of Lip Oral Cavity and Pharynx; Malignant Neoplasms of Male Genital Organs

Keywords

Malignant neoplasms of digestive organs; Malignant neoplasms of female genital organs; Malignant neoplasms of lip oral cavity and pharynx; Malignant neoplasms of male genital organs; Human papilloma virus associated malignancies; HPV; Alisertib; MLN8237; TAK-228; MLN0128

Outcome Measures

Primary Outcomes (1)

• Maximum Tolerated Dose (MTD) of Alisertib and TAK-228 in Participants with Human Papilloma Virus (HPV) Associated Malignancies

  Maximum tolerated dose (MTD) defined by dose limiting toxicities (DLTs) that occur within the initial cycle (21 days).

  21 days

Secondary Outcomes (1)

• Clinical Benefit of Alisertib and TAK-228 in Participants with Human Papilloma Virus (HPV) Associated Malignancies

  6 months

Study Arms (1)

Alisertib + TAK-228

EXPERIMENTAL

Dose Escalation Phase: Starting dose of Alisertib: 30 mg by mouth 2 times a day on Days 1 - 7 each 21 day cycle. Starting dose of TAK-228: 1 mg by mouth daily Days 3 - 18, with the exception of 2 mg daily Days 3 - 7 and 10 - 14 schedule in a 21 day cycle. Dose Expansion Phase: Alisertib and TAK-228 taken at the maximum tolerated dose from Dose Escalation Phase.

Drug: Alisertib; Drug: TAK-228

Interventions

Alisertib DRUG

Dose Escalation Phase: Starting dose of Alisertib: 30 mg by mouth 2 times a day on Days 1 - 7 each 21 day cycle. Dose Expansion Phase: Maximum tolerated dose from Dose Escalation Phase.

Also known as: MLN8237

Alisertib + TAK-228

TAK-228 DRUG

Dose Escalation Phase: Starting dose of TAK-228: 1 mg by mouth daily Days 3 - 18, with the exception of 2 mg daily Days 3 - 7 and 10 - 14 schedule in a 21 day cycle. Dose Expansion Phase: Maximum tolerated dose from Dose Escalation Phase.

Also known as: MLN0128

Alisertib + TAK-228

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients with locally advanced or metastatic HPV associate malignancy (cervical, vaginal, vulvar, penile, anal or oropharyngeal carcinoma), either refractory to standard therapy or for which no effective standard therapy that confers clinical benefit is available.
• Patients must have measurable disease, as defined by RECIST 1.1.
• Male or female patients 18 years or older.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
• For women: - Postmenopausal for at least 1 year before the screening visit, OR - Surgically sterile, OR - If they are of childbearing potential, agree to practice 1 effective methods of contraception and 1 additional effective (barrier) method, at the same time, from the time of signing the informed consent through 90 days (or longer, as mandated by local labeling \[eg. USPI, SmPC, etc;\])after the last dose of study drug OR agree to practice true abstinence, when this is in line with the preferred and usual lifestyle of the patient (Periodic abstinence \[e.g, calendar, ovulation, symptothermal, postovulation methods\] and withdrawal, spermicides only and lactational amenorrhea are not acceptable methods of contraception. Female and male condoms should not be used together.)
• For men, even if surgically sterilized (ie, status post-vasectomy), they must: - Agree to practice highly effective barrier contraception during the entire study treatment period and through 120 days after the last dose of study drug, OR agree to practice true abstinence, when this is in line with the preferred and usual lifestyle of the patient (Periodic abstinence \[e.g, calendar, ovulation, symptothermal, postovulation methods for the female partner\] and withdrawal, spermicides only, and lactational amenorrhea are not acceptable methods of contraception. Female and male condoms should not be used together.) - Agree not to donate sperm during the course of this study or 120 days after receiving their last dose of study drug
• Screening clinical laboratory values as specified: -Bone marrow reserve consistent with: absolute neutrophil count (ANC) \>/= 1.5 x 10\^9/L; platelet count \>/= 100 x 10\^9/L; hemoglobin \>/= 9 g/dL without transfusion within 1 week preceding study drug administration. -Hepatic: total bilirubin \</= 1.5 x upper limit of normal (ULN), transaminases (aspartate aminotransferase/serum glutamic oxaloacetic transaminase-AST/SGOT and alanine aminotransferase/serum glutamic pyruvic transaminase-ALT/SGPT) \</= 2.5 x ULN (\</= 5 x ULN if liver metastases are present); -Renal: creatinine clearance \>/=50 mL/min based either on Cockcroft-Gault estimate or based on urine collection (12 or 24 hour); -Metabolic: Glycosylated hemoglobin (HbA1c)\<7.0%, fasting serum glucose (\</= 130 mg/dL) and fasting triglycerides \</= 300 mg/dL;
• Left ventricular ejection fraction (LVEF) be at least \>/= institutional standard of normal as measured by echocardiogram (ECHO) or multiple gated acquisition scan (MUGA) within 4 weeks prior to first study drug administration
• Ability to swallow oral medications.
• Voluntary written consent must be given before performance of any study related procedure not part of standard medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care.
• Patients who have a history of brain metastasis are eligible for the study provided that all the following criteria are met:-Brain metastases which have been treated, -No evidence of disease progression for \>/= 3 months or hemorrhage after treatment, -Off-treatment with dexamethasone for 4 weeks before administration of the first dosing, -No ongoing requirement for dexamethasone or anti-epileptic drugs

You may not qualify if:

• Other clinically significant co-morbidities, such as uncontrolled pulmonary disease, active central nervous system disease, active infection, or any other condition that could compromise the patient's participation in the study.
• Known human immunodeficiency virus infection.
• Known hepatitis B (they test positive for the presence of at least one of the following three markers in blood (to be evaluated at screening): hepatitis B surface antigen (HBsAG), antibodies against hepatitis B core antigen (anti-HBc), or hepatitis B viral load (HBV DNA), or known active hepatitis C infection.
• Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of treatment according to this protocol.
• Diagnosed or treated for another malignancy within 2 years before administration of the first dose of study drug, or previously diagnosed with another malignancy and have any evidence of residual disease. Patients with nonmelanoma skin cancer or carcinoma in situ of any type are not excluded if they have undergone complete resection.
• Female subject who is pregnant or breast-feeding. Confirmation that the subject is not pregnant must be established by a negative serum b-human chorionic gonadotropin (b-hCG) pregnancy test result obtained during screening. Pregnancy testing is not required for post-menopausal or surgically sterilized women.
• Inability or unwillingness to swallow oral medication. Manifestations of malabsorption due to prior gastrointestinal (GI) surgery, GI disease, or for an unknown reason that may alter the absorption. In addition, patients with enteric stomata are also excluded.
• Therapy with any investigational products within 21 days before the first dose of study drug.
• History of any of the following within the last 6 months before administration of the first dose of the drug:-Ischemic myocardial event, including angina requiring therapy and artery revascularization procedures, -Ischemic cerebrovascular event, including transient ischemic attack and artery revascularization procedures, -Requirement for inotropic support (excluding digoxin) or serious (uncontrolled) cardiac arrhythmia (including atrial flutter/fibrillation, ventricular fibrillation or ventricular tachycardia), -Placement of a pacemaker for control of rhythm, -New York Heart Association (NYHA) Class III or IV heart failure, -Pulmonary embolism
• Significant active cardiovascular or pulmonary disease including: -Uncontrolled hypertension (i.e., systolic blood pressure \>180 mm Hg, diastolic blood pressure \> 95 mm Hg). Use of anti-hypertensive agents to control hypertension before Cycle1 Day 1 is allowed., -Pulmonary hypertension, -Uncontrolled asthma or O2 saturation \< 90% by arterial blood gas analysis or pulse oximetry on room air, -Significant valvular disease; severe regurgitation or stenosis by imaging independent of symptom control with medical intervention, or history of valve replacement, -Medically significant (symptomatic) bradycardia, -History of arrhythmia requiring an implantable cardiac defibrillator, -Baseline prolongation of the rate-corrected QT interval (QTc) (e.g., repeated demonstration of QTc interval \> 480 milliseconds, or history of congenital long QT syndrome, or torsades de pointes)
• Treatment with strong inhibitors and/or inducers of cytochrome P450 (CYP) 3A4, CYP2C9 or CYP2C19 within 1 week preceding the first dose of study drug.
• Receipt of corticosteroids within 7 days prior to the first dose of study treatment, unless patient has been taking a continuous dose of no more than 15 mg/day of prednisone or equivalent for at least 1 month prior to first dose of study treatment. Low dose steroid use for the control of nausea and vomiting, topical steroid use and inhaled steroids are permitted.
• The intermittent use of PPI, H2-antagonists and antacids (including carafate) is only allowed within these guidelines: -PPI until D-5 prior to the first dose of alisertib and prohibited for the duration of the study, -H2 antagonists until D-1 and after the dosing of alisertib is done, -Antacid formulations until 2 hours before dosing and after 2 hours following dosing
• Radiation therapy to more than 25% of the bone marrow. Whole pelvic radiation is considered to be over 25%.
• Prior allogeneic bone marrow or organ transplantation.

Sponsors & Collaborators

• M.D. Anderson Cancer Center: lead
• Millennium Pharmaceuticals, Inc.: collaborator

Related Links

• University of Texas MD Anderson Cancer Center Website

MeSH Terms

Interventions

MLN 8237; sapanisertib

Study Officials

• Siqing Fu, MD, PHD

  M.D. Anderson Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 16, 2016
• First Posted: June 23, 2016
• Study Start: September 1, 2016
• Primary Completion: September 1, 2021
• Last Updated: March 27, 2017

Record last verified: 2017-03