A Phase I Trial of HS-10241 in Solid Tumors

• Status: Completed
• Trial end date: 2018-05-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a phase 1, open-label, dose-escalation trial of HS-10241 as monotherapy in subjects with solid tumors. HS-10241 will be administered orally once daily.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Atridia Pty Ltd.

Criteria

Inclusion Criteria:

1. At least 18 years of age

2. Ability to understand the purposes and risks of the trial and his/her informed consent using the Human Research Ethics Committee (HREC) approved informed consent form (ICF).

3. Histologically or cytologically confirmed advanced or metastatic solid tumor for which standard therapy does not exist, has failed, or has been refused.

4. Recovered from toxicities of prior anti-cancer treatment to Grade 1 or less (except alopecia)

5. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

6. Life expectancy of at least 3 months

7. Acceptable liver function defined below:

• Total bilirubin ≤ 2 times upper limit of normal range (ULN)

• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤3 times ULN; however, ≤5 times ULN in a subject who has liver metastases

8. Acceptable renal function defined below:

• Serum creatinine ≤1.5 times ULN or calculated creatinine clearance (by the Cockcroft-Gault formula) ≥60 mL/minutes

9. Acceptable coagulation status defined below:

• Prothrombin time <1.5 times ULN

• Partial thrombin time <1.5 times ULN

10. Acceptable hematologic status (without hematologic supports including hematopoietic factor, blood transfusion) defined below:

• Absolute neutrophil count (ANC) ≥1500/μL

• Platelet count ≥100000/μL

• Hemoglobin ≥9.0 g/dL

11. No clinically significant abnormalities in urinalysis

12. All participants must agree to use effective means of contraception (surgical sterilization or the use of barrier contraception with either a condom or diaphragm in conjunction with spermicidal gel or an intrauterine device) with their partner from entry into the trial through 6 months after the last dose.

Exclusion Criteria:

1. Hematologic malignancies

2. Cardiac disease with New York Heart Association (NYHA) Class III or IV, including congestive heart failure, myocardial infarction within 6 months prior to the trial entry, unstable arrhythmia, or symptomatic peripheral arterial vascular disease

3. Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy

4. Major surgery, other than diagnostic surgery, within 4 weeks prior to the trial entry, without complete recovery

5. Percutaneous coronary intervention conducted within 6 months prior to the trial entry for cardiac infarction or angina pectoris

6. Seizure disorders requiring anticonvulsant therapy

7. Taking a medication that prolongs QT interval and has a risk of Torsade de Pointes, or a history of long QT syndrome

8. Medical history of difficulty swallowing, malabsorption or other chronic gastrointestinal disease, or conditions that may hamper compliance and/or absorption of the tested product

9. Anti-cancer treatment with radiation therapy, surgery, chemotherapy, targeted therapies (erlotinib, lapatinib, etc.), or immunotherapy within 4 weeks (6 weeks for nitrosoureas or Mitomycin C) prior to trial entry. Ongoing androgen deprivation therapy or bisphosphonates are allowed.

10. Participation in an investigational drug or device trial within 4 weeks prior to the trial entry

11. Known infection with human immunodeficiency virus (HIV), hepatitis B, or hepatitis C

12. Recent venous thrombosis (including deep vein thrombosis or pulmonary embolism within 1 year of trial entry)

13. History of upper gastrointestinal hemorrhage, peptic ulcer disease, or bleeding diathesis;

14. Subject is pregnant (positive serum beta human chorionic gonadotropin [β-HCG] test at Screening) or is currently breast-feeding, their partner anticipates becoming pregnant/impregnating during the trial or within 6 months after receiving the last dose of trial treatment

15. Concomitant disease or condition that could interfere with the conduct of the trial, or that would, in the opinion of the Investigator, pose an unacceptable risk to the subject in this trial

16. History of organ allograft, autologous stem cell transplantation, or allogeneic stem cell transplantation

17. Unwillingness or inability to comply with the trial protocol for any reason

18. Legal incapacity or limited legal capacity

19. Known drug abuse or alcohol abuse

20. Taking a medication that is a moderate or strong inhibitor or inducer of CYP2C9. Patients are eligible if these medications can be stopped or substituted within the screening period.