Study Evaluating Hemay020 In Subjects With Advanced Solid Cancer

NCT02467569 | Terminated Phase 1

• 1 other identifier: Hemay020P1 2014
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to assess the pharmacokinetics，safety and tolerability of Hemay020 and to determine the recommended dose for future Phase II study as well as to obtain preliminary information on the efficacy of Hemay020 in subjects with solid tumors. The study will be conducted in two parts. Part one, testing will be done on up to 16-31 subjects to determine the safety and tolerability of Hemay 020 in patients with advanced solid tumors. Part two, another 16-24 subjects with advanced or metastatic NSCLC, will be added to the trial to better define the tolerability and preliminary efficacy of Hemay020.

Conditions

Neoplasms，Non-Small Cell Lung Cancer

Outcome Measures

Primary Outcomes (6)

• Number of participants with adverse events

  At screening, weekly up to 18 months

• Observed maximum concentration of Hemay020

  0, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, 72, 96, 144 hours post-dose on day 1 and day 42

• Time of maximum concentration of Hemay020

  0, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, 72, 96, 144 hours post-dose on day 1 and day 42

• Area under the plasma concentration versus time curve of Hemay020

  0, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, 72, 96, 144 hours post-dose on day 1 and day 42

• Trough Plasma Concentrations of Hemay020

  0, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12, 24, 36, 48, 72, 96, 144 hours post-dose on day 1 and day 42

• Predose plasma concentration

  Predose on day 8, 15, 22]

Secondary Outcomes (2)

• Disease control rate (complete response rate + partial response rate + stable disease rate) according to RECIST v1.1

  At screening, after 4 weeks of treatment

• Objective response rate (complete response rate + partial response rate) according to RECIST v1.1

  At screening, after 4 weeks of treatment

Study Arms (1)

Hemay020

EXPERIMENTAL

Part one: Dose Escalation Group Hemay020 capsules will be taken orally in doses of 25mg, 50mg, 100mg, 200mg or 300mg once daily for 28 days. Part two: Extension Group Hemay020 capsules will be taken in two dose groups that assessed by Part one for 28 days.

Drug: Hemay020

Interventions

Hemay020 DRUG

Hemay020

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female subjects aged 18 to 70 years;
• Subjects with histologically or cytologically confirmed diagnosis of solid tumor; and subjects who have failed standard therapy，or no effective therapy available for such patients;
• at least one measurable tumour lesion (non radiation field) as defined by RECIST criteria and measured by CT or MRI techniques;
• Patients have received chemotherapy at least 4 weeks prior to screening and must have recovered from any toxic effects of the treatment to CTCAE≤Grade 1;
• Part 1 Only: ECOG Performance Status of 0,1;
• Life expectancy of at least three (3) months;
• Adequate bone marrow, liver, kidney and coagulation function, meeting the following criteria:
• ANC≥1.5×109/L，HB≥90g/L，PLT≥75×109/L； TBIL≤2×ULN； ALT≤2.5×ULN，AST≤2.5×ULN（ALT≤5×ULN，AST≤5×ULN if liver metastases are present） Serum creatinine≤1.5×ULN INR≤1.5×ULN Patients without gastrointestinal tract disease, which results in malabsorption syndrome, or patients who are unable to take oral medication;
• All female and male subjects must agree and commit to the use of two contraceptive regimen for the duration of the study and for 6 months after the last dose of test article. Female subjects must have a negative serum or urine pregnancy test performed within 72 hours prior to treatment. Male subjects's sexual partner must use two contraceptive regimen.
• Two contraceptive regimens include a medication and non-medication contraceptive regimen;
• Able to understand and sign a written informed consent before study entry;
• Histological or cytological diagnosis of EGFR wild-type (or genetype is not determined) patients, with advanced or metastatic lung cancer after receiving two chemotherapy; or advanced or metastatic patients with EGFR mutation after receiving EGFR-TKI and one chemotherapy.
• ECOG Performance Status of 0,1,2

You may not qualify if:

• Patients with parenteral nutrition; malabsorption syndrome; any condition possibly affecting drug absorption or inability to tolerate oral medications;
• Immunodeficiency history, including human immunodeficiency HIV positive（by ELISA and Western Blot）;
• clinically QTc prolongation, ventricular tachycardia, ventricular fibrillation, heart block, myocardial infarction within 1 year, congestive heart failure, symptoms requiring medicine treatment patients with coronary heart disease;
• Left ventricular ejection fraction (LVEF) \<40％;
• active infection (ie, requiring intravenous antibiotic or antiviral agent);
• Organ or system status:
• Patients with brain metastasis untreated surgical resection or radiotherapy, Patients with treated brain metastasis may be excluded if they are neurologically unstable and have been on steroids or receiving steroids less than 4 weeks prior to study;
• Patients with bone marrow metastasis;
• Documented history of interstitial lung disease, drug induced interstitial lung disease, radiation pneumonitis with steroids treatment, any evidence of clinically active interstitial lung disease;
• Idiopathic fibrosis of the lung by CT scan before study entry;
• Presence of clinically significant or uncontrolled disease (ie. unstable or uncompensated respiratory, heart, liver, kidney disease) in the investigator's judgment;
• Any unstable systemic disease(including severe hypertension, unstable angina, congestive heart failure, liver and kidney or metabolic disease)
• Any other malignant cancer within 5 years with the exception of adequately treated cervical cancer in situ or basal and squamous cutaneous cell carcinomas
• Neurological and psychogenic disorders, including epilepsia or dementia;
• Major surgery (not including biopsy) or injury within 4 weeks of treatment day 1;

Sponsors & Collaborators

• Tianjin Hemay Pharmaceutical Co., Ltd: lead
• Hainan General Sanyang Pharmaceutical Co., Ltd: collaborator

Study Sites (1)

Sun Yat-Sen University Cancer Centre

Guangzhou, Guangdong, 510060, China

Location

Study Officials

• Haiying Wu, Professor

  Sun Yat-sen University Cancer Centre

  PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

• First Submitted: June 2, 2015
• First Posted: June 10, 2015
• Study Start: July 3, 2015
• Primary Completion: December 31, 2017
• Study Completion: December 31, 2017
• Last Updated: March 1, 2024

Record last verified: 2024-02

Locations

CN (1)