A Phase 1, Open-label, Multiple Dose Escalation Trial to Determine Safety and Tolerability of Once Daily OPB-111077 in Subjects With Advanced Cancer

A Phase 1, Open-label, Multiple Dose Escalation Trial to Determine Safety and Tolerability of Once Daily OPB-111077 in Subjects With Advanced Cancer

The primary objective of this study is to determine the safe and tolerable dose level of OPB-111077 for patients with advanced cancer.

The secondary objective of this study is to investigate the pharmacokinetic properties of OPB-111077; the pharmacodynamic effects of OPB-111077; the antitumor activity of OPB-111077 as assessed by RECIST or IMWG Uniform Response Criteria; and to explore whether PET responses correlate with other measures of clinical response.

Inclusion Criteria:

• Pathologically and/or cytologically confirmed advanced malignancy that is refractory to standard therapy or for which there are no standard treatment options available

• For oral or intravenous anticancer therapies, at least 4 weeks or 5 half-lives, whichever is shorter, need to have elapsed since the last dose

• Recovery from adverse effects of prior therapy at time of enrollment to

  o ≤ Grade 1 (excluding alopecia)

• Agreement to forego any other chemotherapy, immunotherapy, radiotherapy, or investigational drug while enrolled on this trial except hormonal therapy for prostate cancer or radiotherapy for symptomatic bone metastases known to be present at Screening

• Male or female subjects aged ≥ 18 years

• ECOG performance status ≤ 2

• Adequate organ function

• Life expectancy of ≥ 3 months following trial entry

• For women of childbearing potential, a negative serum pregnancy test result at Screening

• For women of childbearing potential or men whose sexual partners are women of childbearing potential, agreement to use 2 methods of adequate contraception prior to trial entry, for the duration of the trial, and for 90 days after the last dose of trial medication

• Signed and dated IRB-approved informed consent prior to any performance of protocol-specific screening procedures

Exclusion Criteria:

• Uncontrolled concurrent illness, including but not limited to: ongoing or active infection; uncontrolled heart, liver, kidney, or endocrine disorder
• Altered mental status, psychiatric illness, or social situation that would limit compliance with trial requirements and/or obscure trial results
• Immunocompromised state
• Known or evidence of chronic viral hepatitis (hepatitis B or C virus)
• Untreated or symptomatic brain metastasis, or subjects with leptomeningeal disease
• Inability to swallow oral meds or gastrointestinal disorder that might interfere with absorption of oral drugs
• Major surgery within 28 days of first receipt of trial drug
• Nursing or pregnant women
• ≥ Grade 1 neuropathy with pain or > Grade 2 neuropathy without pain (subjects with neuropathy caused by a previous regimen that is recovered to ≤ Grade 2 and stable without pain may be included)
• Food-effect sub-study (Part B) only: Pathologies or medical histories that might impair absorption and elimination.
• PET scan sub-study (Part C) only: Uncontrollable blood glucose or intolerance to PET scan procedures.