Study of AR-12 (2-Amino-N-[4-[5-(2 Phenanthrenyl)-3-(Trifluoromethyl)-1H-pyrazol-1-yl] Phenyl]-Acetamide) in Adult Patients With Advanced or Recurrent Solid Tumors or Lymphoma

Completed · Phase 1

Conditions studied: Solid Tumors, Lymphoma

In brief

The primary objective of this study in adults with advanced or recurrent solid tumors or lymphoma is to evaluate the safety and tolerability of AR-12 by describing dose-limiting toxicities (DLTs), and thereby establishing the maximum tolerated dose (MTD) or, in the absence of reaching an MTD, a recommended dose (RD) for additional study of oral AR-12 administered daily in cycles of 28 days (28 consecutive days of once daily treatment with at least a 7-day break between the first and second treatment cycles and recovery of toxicity to grade 1 or less, with no planned off-treatment days between subsequent cycles).

Key facts

Study ID: NCT00978523
Run by: Arno Therapeutics
People needed: 35
Starts: 2009-08-01
Expected to finish: 2013-11-01
Last updated by the study team: 2014-01-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Signed, written informed consent must be obtained and documented according to International Conference on Harmonisation (ICH) Good Clinical Practice (GCP), the local regulatory requirements, and the permission to use private health information in accordance with the Health Insurance Portability and Accountability Act (HIPAA) prior to study-specific Screening procedures.
Both men and women and members of all races and ethnic groups are eligible for this trial.
Patients must be 18 years of age or greater.
Patients must have a histologically or cytologically confirmed advanced or recurrent solid tumor or lymphoma for which standard curative or palliative measures do not exist or are no longer effective. Patients who have recurrent disease after previous surgery, radiation therapy, and/or chemotherapy are eligible. No restriction is placed on the number of prior therapies. At least 4 weeks must have elapsed since the completion of prior therapy, including major surgery, and patients must have recovered from all associated toxicities no greater than grade 1 at the time of Screening. Patients with prostate cancer must have discontinued anti-androgens (eg, bicalutamide, nilutamide) for at least 6 weeks; chemical castration with LHRH analogues can be continued.
Patients must have measurable or evaluable disease or disease that otherwise meets criteria for treatment and can be followed by an acceptable biomarker (eg, PSA or CA-125) documented within 28 days of starting treatment with AR-12. Pleural effusions, ascites, bony metastasis, and laboratory parameters are not acceptable as the only evidence of disease.
Patients must have acceptable organ and marrow function documented within 7 days of registration, defined as follows:
Leukocytes >3,000/mcL
Absolute neutrophil count >1,500/mcL
Platelets ≥150,000/mcL
Fasting blood glucose Within normal institutional limits
Total bilirubin Within normal institutional limits
AST/ALT <2.5 X institutional ULN; <5 X ULN in presence of liver metastasis
Creatinine Within normal institutional limits, OR
Creatinine clearance >60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal
Patients must have an ECOG performance status of 0 or 1.
Patients must have adequate pulmonary function (no more than a grade 2 finding per CTCAE version 3) and oxygen saturation ≥93% on room air, measured within 14 days prior to initiation of treatment with AR-12.
All patients who are sexually active must use a medically acceptable, as judged by the investigator, and highly effective method of birth control for the duration of the study and to continue for 30 days after the last AR-12 dose. A highly effective method of birth control is defined as any method that results in a low failure rate, including implants, injectables, some intrauterine devices, sexual abstinence, and surgical sterilization (eg, vasectomy, tubal ligation, hysterectomy). Women of childbearing potential must have a negative serum pregnancy test documented within 7 days prior to Day 0. Furthermore, male study patients must also not donate sperm from Study Day 1 until 90 days after the end of treatment.
Patients must have a life expectancy of greater than 12 weeks.

You may not qualify if…

Patients must not have had chemotherapy, radiotherapy, immunotherapy, or investigational agents within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study. Patients who have received prior chemotherapy must have recovered to no greater than grade 1 from all AEs/toxicities (except alopecia) due to prior agents.
Patients with a history of insulin- or non-insulin-dependent diabetes requiring antidiabetic medication.
Patients requiring treatment with anticoagulants.
Patients requiring chronic corticosteroids (dose equivalent ≥20 mg prednisolone).
Patients requiring chronic Celebrex® (celecoxib) therapy.
History of allergic reactions attributed to compounds of similar chemical or biologic composition (eg, celecoxib).
Patients who are unable or unwilling to swallow AR-12 capsules daily or who have any concurrent medical condition that may impact drug absorption, including a history suggestive of intermittent tumor-associated bowel obstruction, and partial small bowel resection.
Patients with known or symptomatic brain metastases (including leptomeningeal disease). Patients with asymptomatic, treated brain metastases are allowed. Patients with primary brain tumors will be allowed in the MTD expansion cohort; however, radiotherapy must have been completed ≥90 days prior to Screening.
Patients with any other prior malignancy are not allowed except for the following:
Adequately treated basal cell or squamous cell skin cancer
In situ cervical cancer
Adequately treated Stage I or II cancer from which the patient is currently in complete remission or other cancer from which the patient has been disease-free for 2 years
Patients may have had prior palliative radiation therapy; however, radiation must not have been to more than 15% of marrow-producing locations.
Pregnant women are excluded from this study because the potential for teratogenic or abortifacient effects of AR-12 are not known. Because there is an unknown but potential risk for AEs in nursing infants secondary to treatment of the mother with AR-12, breastfeeding should be discontinued if the mother is treated with AR-12.
Patients with known human immunodeficiency virus (HIV) are not eligible for this study.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Patients with QTc > 470 msec on Screening ECG or a clinically relevant ECG abnormality as determined by the investigator or his/her designee.
Patients with left bundle-branch block.

Where it is running

TGen Clinical Research Services at Scottsdale Healthcare — Scottsdale, Arizona, United States
The Ohio State University - Comprehensive Cancer Center — Columbus, Ohio, United States
Royal Marsden Hospital — Sutton, Surrey, United Kingdom

Full record on ClinicalTrials.gov

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