A Study Evaluating Enzalutamide Pharmacokinetics and Pharmacodynamics, and Related Changes After Drug Switch

NCT03778047 | Completed Phase 1

• 1 other identifier: HC-1119-02
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 1

Brief Summary

This is a study for evaluating enzalutamide pharmacokinetics and pharmacodynamics, and related changes after drug switch in Chinese patients with metastatic castration-resistant prostate cancer. The study primary objective is to evaluate the pharmacokinetic characteristics of enzalutamide in Chinese patients with mCRPC.

Conditions

Metastatic Castration Resistant Prostate Cancer

Outcome Measures

Primary Outcomes (3)

• Maximum drug concentration(Cmax)

  From the first dose of the study drug to 12 weeks after dose

• Time of maximum drug concentration(Tmax)

  From the first dose of the study drug to 12 weeks after dose

• Area under curve from time 0 to 24h (AUC0-24h)

  From the first dose of the study drug to 12 weeks after dose

Secondary Outcomes (5)

• Maximum drug concentration(Cmax)

  From 13 weeks to 24 weeks after dose

• Time of maximum drug concentration(Tmax)

  From 13 weeks to 24 weeks after dose

• Area under curve from time 0 to 24h (AUC0-24h)

  From 13 weeks to 24 weeks after dose

• Number of patients with adverse events

  From the first dose of the study drug to 24 weeks after dose

• Percentage of patients with > 50% decrease in prostate specific antigen (PSA)

  From the first dose of the study drug to 12 weeks after dose

Study Arms (2)

enzalutamide

EXPERIMENTAL

160mg

Drug: Enzalutamide

HC-1119

EXPERIMENTAL

To be determined

Drug: HC1119

Interventions

Enzalutamide DRUG

oral

enzalutamide

HC1119 DRUG

oral

HC-1119

Eligibility Criteria

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

You may qualify if:

• Voluntarily participated in the study, with understanding of and will to comply with relevant study procedures and signed informed consent form;
• Chinese male, ≥ 18 years old;
• With histologically or cytologically confirmed prostate cancer, without neuroendocrine carcinoma or ductal adenocarcinoma;
• With evidence of metastatic lesions (such as bone scan and CT/MRI);
• Patients with relapsed, refractory, or progressive disease despite castration (surgery or chemical) or combined androgen deprivation therapy. (Progressive disease is defined as 1 or more of the following 3 criteria: PSA progression: A minimum of 3 rising PSA values with an interval of at least 1 week between determinations, resulting in a final value higher than 50% of the minimum, with a starting PSA value \> 2 ng/ml; Soft tissue disease progression as defined by RECIST 1.1; Bone progression as defined by PCWG2 with 2 or more new lesions on bone scan);
• Castrate levels of testosterone (\< 50 ng/dl) at screening; bilateral orchiectomy or ongoing androgen deprivation therapy with effective GnRH analogues;
• ECOG performance status ≤1;
• Laboratory tests must meet the following criteria:
• Routine Blood Test: hemoglobin (Hb) ≥ 90g/L (no blood transfusions within 14 days prior to screening); absolute neutrophil count (ANC) ≥ 1.5 x 109/L; Platelet Count (PLT) ≥ 80 x 109/L;
• Blood Biochemistry: creatinine (Cr) ≤ 2 x upper limit of normal (ULN), or Cr \> 2 x ULN but the calculated CrCl ≥ 60 ml/min; bilirubin (BIL) ≤2 x ULN; alanine aminotransferase (ALT), aspartate aminotransferase (AST) ≤2.5 x ULN (or ≤ 5.0 x ULN for patients with liver metastases);
• Coagulation: INR \< 1.5.
• Estimated life expectancy \> 6 months.

You may not qualify if:

• Participated in other clinical drug trials within 1 month prior to screening, or the occurrence of toxicity caused by previous treatments that has not been relieved to ≤ Grade 2 toxicity (according to CTCAE 4.03) prior to enrollment;
• Brain metastases;
• Subjects are excluded if any of the following conditions are met:
• Other malignancies within the last 5 years (except for curatively treated non-melanoma skin cancer);
• History of organ transplants;
• Past medical history of seizures, serious CNS diseases, or unexplained coma, family history of seizures, or history of traumatic brain injury;
• Uncontrolled hypertension (systolic ≥ 160 mmHg or diastolic ≥ 100 mmHg) or other serious cardiovascular diseases. (Patients with a history of hypertension is eligible if his blood pressure is controlled with antihypertensives);
• Significant GI dysfunction which may affect the intake, transport, or absorption of drug (such as inability to swallow, chronic diarrhea, and bowel obstruction, etc.), or patients with complete gastrectomy;
• Other uncontrolled clinical diseases, including but not limited to: persistent or active infections.
• Subjects are excluded if any of the following conditions regarding past or concomitant medication are met:
• Medications that lower the seizure threshold must be used during the trial;
• Treatment with 5α-reductase inhibitors (finasteride, dutasteride), estrogen, or cyproterone within 4 weeks prior to screening;
• Treatment with ketoconazole within 4 weeks prior to screening;
• Previously treated with investigational or approved medications that inhibit testosterone synthesis (such as abiraterone acetate, TAK-683, and TAK-448) or target testosterone receptors (such as SHR3680, proxalutamide, and ARN509), except for bicalutamide and flutamide.
• Known hypersensitivity to any ingredient of the study drugs (enzalutamide and HC-1119) or similar drugs;

Sponsors & Collaborators

• Hinova Pharmaceuticals Inc.: lead

Study Sites (1)

Medical Ethics Committee of Hunan Cancer Hospital

Changsha, China

Location

MeSH Terms

Interventions

enzalutamide

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 11, 2018
• First Posted: December 19, 2018
• Study Start: February 7, 2018
• Primary Completion: October 24, 2018
• Study Completion: August 28, 2019
• Last Updated: November 3, 2020

Record last verified: 2020-10

Locations

CN (1)