Study of CS3006 in Subjects With Locally Advanced or Metastatic Solid Tumors

Locally Advanced or Metastatic Solid Tumors Clinical Trial

Official title:

A Phase I, Open Label, Multiple Dose, Dose Escalation and Expansion Study to Investigate the Safety, Tolerability, Pharmacokinetics and Antitumor Activities of the MEK Inhibitor CS3006 in Subjects With Locally Advanced or Metastatic Solid Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03736850
• Other study ID #: CS3006-102
• Status: Completed
• Phase: Phase 1
• Start date: October 19, 2018
• Est. completion date: May 15, 2020

Study information

• Verified date: March 2020
• Source: CStone Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multicenter, open label, sequential-cohort, dose escalation & expansion phase I study to evaluate the clinical safety, tolerability, PK, and preliminary efficacy of CS3006 and to establish the Maximum Tolerated Dose (MTD）, if any, Recommended Phase II Doses (RP2Ds) and regimen of CS3006. The study is composed of two parts: Part 1 for dose escalation and Part 2 for dose expansion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 17
• Est. completion date: May 15, 2020
• Est. primary completion date: May 15, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Willing and able to provide written informed consent for the trial.

2. Subjects must have a histologically or cytologically confirmed advanced or metastatic solid tumor(s) for which no effective standard therapy is available or tolerable.

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

4. Life expectancy = 12 weeks.

5. Able to swallow and retain oral medication.

6. Subject must have adequate organ function.

7. Use of effective contraception.

Exclusion Criteria:

1. Subjects receiving cancer therapy at the time of enrollment.

2. Has had prior chemotherapy, targeted therapy, immunotherapy or any other agents used as systemic treatment for cancer, within 14 days of the first dose of investigational product administration or who has not recovered from adverse events due to a previously administered agent.

3. Previous treatment with a MEK inhibitor.

4. Use of any investigational anti-cancer drug within 28 days before the first investigational product administration.

5. Current use of a prohibited medication.

6. Presence of active gastrointestinal disease or other condition that will interfere significantly with the absorption, distribution, metabolism, or excretion of drugs.

7. Known brain metastasis or other CNS metastasis that is either symptomatic or untreated.

8. Primary malignancy of the central nervous system.

9. Evidence of severe or uncontrolled systemic diseases.

10. Subjects with clinically significant cardiovascular disease.

11. Human Immunodeficiency Virus (HIV) infection.

12. Subjects with active Hepatitis B or C infection.

13. Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the investigational product or excipients.

14. Concurrent condition that in the investigator's opinion would jeopardize compliance with the protocol.

15. Unwillingness or inability to follow the procedures outlined in the protocol.

For more information regarding trial participation, please contact at cstonera@cstonepharma.com

Related Conditions & MeSH terms

• Locally Advanced or Metastatic Solid Tumors
• Neoplasms

Intervention

Drug:
• CS3006
In the dose escalation part, the dose levels will be escalated following a modified 3+3 dose escalation scheme. In the dose expansion part, participants will receive CS3006 at specified dose level(s).

Locations

Country	Name	City	State
China	People's Liberation Army 307 Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
CStone Pharmaceuticals

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with adverse events		From the day of first dose to 30 days after last dose of CS3006