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Dose-Escalation and Efficacy Study of LAE001 / Prednisone Plus Afuresertib Patients With m-CRPC

Trial Status: Active

The combination treatment of protein kinase B (AKT) inhibitor, afuresertib, with androgen synthesis enzyme inhibitor, LAE001, may provide an effective treatment for metastatic castration resistant prostate cancer (m-CRPC) patients who have progressed / drug resistant following prior standard care treatments of any anti-androgen. This study intends to identify the most appropriate combined doses of LAE001 / prednisone and afuresertib in m-CRPC patients who have progressive disease or are intolerant of 2 prior standard treatments of any anti-androgen or anti-androgen treatment plus chemotherapy.

Inclusion Criteria

  • Patients, males ≥18 years of age, must be able to provide written informed consent.
  • Patients must have documented histological or cytological evidence of adenocarcinoma of the prostate (excluding neuroendocrine differentiation or small cell histology).
  • Patients must have radiographic evidence of metastatic disease based on RECIST 1.1 within the 28 days before enrollment.
  • Patients are able to provide tumor biopsy samples for PTEN immunohistochemical (IHC) staining. A valid PTEN IHC result must be collected within 4 months of screening visit or from a fresh biopsy sample during screening visit. The PTEN ICH results should be either performed or confirmed, if there is a previous PTEN ICH result, by central laboratory testing (participants with an "invalid" or "failed" PTEN IHC result are not permitted to be enrolled in Phase II study but allowed to participate in Phase I study).
  • Patients must have progressive disease based on the PCWG3 criteria:
  • Patients who progressed based solely on total PSA rising, should have had a sequence of rising values on 3 consecutive occasions of at least 1-week intervals (if the third measurement is not greater than the second measurement, a fourth measurement at least a week apart must be taken and must be greater than the second measurement) and should have 2.0 ng/mL minimum level for entry.
  • Patients who have documented disease progression per RECIST 1.1 are eligible independent of PSA.
  • Patients with bone only progression according to PCWG3 (ie, bone scan showing appearance of ≥2 new lesions). Note: Patients must have had a prior PSA response, followed by documented PSA progression on prior hormone treatment.
  • Patients must have castration levels of testosterone (<50 ng/dL or 1.7 nmol/L). Note: Patients must have undergone androgen deprivation therapy (ADT), such as orchiectomy, or have been on Luteinizing Hormone Releasing Hormone (LHRH) agonists or antagonists, for at least 3 months prior to study enrollment. Patients on LHRH agonists/antagonists must remain on these agents for the duration of the study.
  • Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1.
  • Patients must have adequate hematopoietic function by local laboratory within the 28 days before enrollment, as evidenced by:
  • Absolute neutrophil count ≥1,500/μL
  • Platelet count ≥75,000/μL
  • Hemoglobin ≥9 g/dL
  • Total serum bilirubin ≤1.5 × Upper Limit of Normal (ULN) within the 28 days before enrollment (in patients with known Gilbert's syndrome, total bilirubin ≤3 × ULN with direct bilirubin ≤1.5 × ULN).
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5 × ULN except for patients with tumor involvement of the liver who must have AST and ALT ≤5 × ULN within the 28 days before enrollment.
  • Patients must have adequate renal function as evidenced by a serum creatinine of ≤1.5 × the ULN for the reference laboratory or creatinine clearance ≥50 mL/min within the 28 days before enrollment (calculated from Cockcroft-Gault formula or 24-hour urine collection).
  • Serum potassium ≥3.5 mmol/L and < ULN within the 28 days before enrollment.
  • Fasting glucose ≤120 mg/dL or ≤6.7 mmol/L; glycosylated hemoglobin ≤8% within the 28 days before enrollment.
  • Patients who have mCRPC progressed or are intolerant after receiving 2 prior treatments of any anti-androgen (such as abiraterone, enzalutamide, apalutamide, or any other Adrenergic Agonist (AR) antagonists that are approved later), or one of the above anti-androgen treatments plus one of the chemotherapies from docetaxel or cabazitaxel. Patients must have at least 3 weeks of treatment of any antiandrogen and/or completed at least 4 Cycles of docetaxel or cabazitaxel treatment before their screening visit.
  • Concomitant use of bisphosphonates and other bone supportive agents is allowed if the dose and renal function have been stable for at least 12 weeks before enrollment and no related ≥Grade 2 side effects are present for at least 4 weeks prior to study drug treatment. The minimum washout period is 4 weeks for prostate cancer therapy (cytotoxic, biologic, other therapies), and 6 weeks for antiandrogens bicalutamide and MDV3100 before enrollment, starting from the day the therapies were stopped.
  • Patients with a female partner of childbearing potential must agree to use condoms plus an additional contraceptive method to avoid conception until the end of relevant systemic exposure plus 90 days following the Clinical Trial Facilitation Group contraception guideline from September 2014.
  • Patient should be able to swallow and retain oral medication and should not have any known gastrointestinal diseases that may interfere with drug absorption.
  • Life expectancy of at least 6 months.

Exclusion Criteria

  • Major surgery within 28 days before study treatment and/or have not recovered fully from the adverse effects of any major surgical procedures before study treatment.
  • Patients that received other second-line Androgen Deprivation Therapy (ADT) (including but not limited to ketoconazole and amino glutethimide) within 6 weeks before enrollment.
  • Patients who have completed sipuleucel-T (Provenge®) treatment within 3 months of enrollment.
  • Patients who have received antiandrogens such as flutamide (EULEXIN®), bicalutamide (CASODEX®), or nilutamide (NILANDRON®) for >3 months must be off treatment for 6 weeks prior to enrollment and should demonstrate a continued rise in PSA after withdrawal.
  • Patients on 5-alpha reductase inhibitors such as finasteride (PROSCAR®, PROPECIA®), or dutasteride (AVODART®) must stop medication at least 3 months prior to enrollment.
  • Patients who have received Radium Ra 223 dichloride (XOFIGO®) or Samarium Sm 153 lexidronam (QUADRAMET®) must be off therapy for at least 3 months prior to enrollment.
  • Patients that are currently receiving increasing or chronic treatment (>5 days) with corticosteroids or another immunosuppressive agent, other than daily use of up to 10 mg prednisone (or equivalent) or low-dose steroid for the control of nausea and vomiting, topical steroid, or inhaled steroid use.
  • Patients who require potassium-wasting diuretics. 9. Patients who have received any investigational agent beyond those indicated for the treatment of prostate cancer within 5 half-lives of the agent; if the half-life of the agent is not known, the patients must be off investigational therapy for 4 weeks prior to enrollment.
  • Patients who have received palliative and other radiotherapy within 4 weeks of study enrollment.
  • Patients with symptomatic or known central nervous system metastases from prostate cancer or who are at high risk for spinal cord compression, per investigator's judgment.
  • Patients with a history of hypothalamus, pituitary or adrenal insufficiency.
  • Patients with diabetes mellitus that require insulin at study enrollment. 14. History of another primary malignancy that is currently clinically significant or currently requires active intervention.
  • Inadequately controlled hypertension (eg, systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥95 mmHg) or hypotension (eg, systolic blood pressure ≤80 mmHg or diastolic blood pressure ≤50 mmHg) after up to 3 measurements with at least 5 minutes apart during 28 days before study enrollment.
  • Patients with active cardiac disease or a history of cardiac dysfunction including any of the following:
  • Severe or unstable angina pectoris or acute coronary syndrome or stroke within 6 months prior to study enrollment.
  • Symptomatic pericarditis.
  • Documented myocardial infarction or arterial thrombotic events within 6 months prior to study enrollment.
  • History of documented congestive heart failure (New York Health Association functional classification III to IV).
  • Documented history of cardiomyopathy.
  • Known left ventricular ejection fraction <50% as determined by multiple gated acquisition scan or echocardiogram within 28 days prior to enrollment.
  • History of clinically significant cardiac arrhythmias, as determined by the investigator.
  • Patients with a Fridericia-corrected QT (QTcF) interval of >450 msec on the screening electrocardiogram (ECG) (using the QTcF formula), has a short/long QT syndrome, or history of QT prolongation/Torsades de Pointes.
  • Patients with a history of an active infection (viral, bacterial, or fungal) requiring systemic therapy within 10 days before enrollment, including but not limited to tuberculosis.
  • Patients who have active human immunodeficiency virus (HIV), hepatitis B, or hepatitis C infections.
  • Patients that are currently receiving treatment with drugs known to be moderate or strong inhibitors or inducers of isoenzyme CYP1A (including but not limited: α-Naphthoflavone, Furafylline, Omeprazole, Lansoprazole) and isoenzyme CYP3A (including but not limited: Itraconazole, Ketoconazole, Azamulin, Troleandomycin, Verapamil, Rifampicin). The patients must have discontinued moderate or strong inducers for at least 2 weeks prior to study enrollment and must have discontinued moderate or strong inhibitors for at least 1 week before study enrollment. Spironolactone, Strong bile salt export pump (BSEP) inhibitors, grapefruit juice, herbal medicines such as St. John's wort, Kava, ephedra, gingko biloba, dehydroepiandrosterone, yohimbe, saw palmetto and ginseng should be discontinued.
  • Sexually active males not willing to use a condom during the whole course of the study and for 16 weeks after stopping treatment. Male patients must not father a child in this period. A condom is required to be used also by vasectomized men as well as during intercourse with a male partner in order to prevent delivery of the drug via seminal fluid.
  • Patients with any other medical, psychiatric, or social condition, including substance abuse, which in the opinion of the investigator, would preclude participation in the study.
  • Patients with a history of upper gastrointestinal bleeding or peptic disease in the previous 6 months.
  • Patients have previously received AKT or PI3 kinase pathway or mTOR inhibitors.
  • Any condition that in the assessment of the investigator renders the patient not suitable for participation in this clinical study protocol

Texas

San Antonio
Cancer Therapy and Research Center at The UT Health Science Center at San Antonio
Status: ACTIVE
Contact: Sonia Lisa Creighton
Phone: 210-450-1366

The Phase I part of this study will perform a dose-escalation to identify the recommended

Phase II dose of LAE001/prednisone plus afuresertib in m-CRPC patients.

In the Phase II part of this study, the anti-tumor efficacy of LAE001/prednisone plus

afuresertib and of afuresertib alone will be assessed in m-CRPC patients with Phosphatase and

tensin homolog (PTEN) loss who have progressed on, or who are intolerant of, 2 prior standard

treatments of any anti-androgen or one anti-androgen treatment plus one of the chemotherapy

from docetaxel or cabazitaxel. These study results will provide preliminary efficacy and

safety information of the combination of LAE001/prednisone plus afuresertib and afuresertib

alone.

Trial Phase Phase I/II

Trial Type Treatment

Lead Organization
Laekna Limited

  • Primary ID LAE201INT2101
  • Secondary IDs NCI-2020-03668
  • Clinicaltrials.gov ID NCT04060394