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NCT Number: NCT05749432

A Phase I Study of Hemay181 in Patients With Advanced Solid Tumors

The study will be conducted in about 51 participants in total. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic profile and preliminary antitumor efficacy of Hemay181 in patients with advanced solid tumors.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Beijing Cancer Hospital

Beijing, Beijing Municipality, China

Location status: Recruiting

Location contact

Huiping Li

CONTACT

[email protected]

13811012595

About this study

The primary purpose of this study is to evaluate the safety and tolerability of Hemay181 in patients with advanced solid tumors, and to explore the maximum tolerated dose. The secondary purpose is to evaluate the pharmacokinetic profile of Hemay181 in patients with advanced solid tumors and to evaluate the preliminary evaluation of the anti-tumor efficacy of Hemay181.

The study will be conducted in two parts. Part one, trial will be conducted in about 24 subjects to determine safety and tolerability of Hemay181 in patients with advanced solid tumors. Part two, approximately 15-27 additional subjects with advanced solid tumors are included to better define the tolerability and preliminary efficacy of Hemay181.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female subjects aged 18 to 65 years;
  • Subjects must give informed consent to the study before the study entry and voluntarily sign a written informed consent form;
  • Advanced solid tumors patients that confirmed by pathology (histology or cytology) with adequate standard therapy failure or currently have no effective standard treatment (such as breast, liver, lung, gastric cancer, colorectal cancer, etc.); Standard therapy failure is defined as: patients who have undergone at least 2 lines of standard antineoplastic therapy after recurrence/metastasis (including treatment-naïve stage IV) (if only 1-line therapy is recommended for the tumor, standard 1-line therapy shall prevail), and who have been confirmed by the investigator or have a clear disease progression or are intolerable by the medical history;
  • At least one lesion that can be evaluated by CT/MRI (measurable lesions are required) and meet the reproducible evaluation requirements in RECIST V1.1;
  • At least 4 weeks after the latest treatment (chemotherapy, targeted therapy, immunotherapy, radiotherapy, and/or major surgery, etc.), at least 2 weeks after endocrine therapy, and have recovered from the toxic effects caused by previous treatment to lower than grade 1 (CTCAE version 5.0) [patients with hair loss (any grade), pigmentation (any grade), peripheral sensory neuropathy (grade ≤2) can be enrolled];
  • Eastern Cooperative Oncology Group(ECOG) score of 0,1;
  • Life expectancy of at least three months;
  • Adequate bone marrow, liver, kidney function, meeting the following criteria:

ANC≥1.5×10^9/L, HB≥90g/L, PLT≥75×10^9/L; ALT≤2.5×ULN, AST≤2.5×ULN with no liver metastasis, or ALT≤5×ULN, AST≤5×ULN with liver metastasis; TBIL≤1.5×ULN; Serum creatinine ≤1.5×ULN;

  • All female and male subjects must agree and commit to the use of a reliable contraceptive regimen for the duration of the study and for at least 12 weeks after at the last dose of test article.

Exclusion criteria

  • Pregnant or lactating women;
  • Patients with known central nervous system metastatic disease;
  • Positive blood for human immunodeficiency virus (HIV antibody); Positive hepatitis B surface antigen and Hepatitis B virus deoxyribonucleic acid (HBV-DNA)>upper limit of normal; Active hepatitis C virus (HCV) infection;
  • Patients with active infection requiring intravenous anti-infective therapy;
  • Patients with a history of irinotecan allergic reactions or previous irinotecan gastrointestinal toxicity ≥ grade 3;
  • Have received drug therapy from other clinical trials within 4 weeks prior to enrollment;
  • Known allergy to the active ingredient or excipients of the test drug;
  • The investigator believes that the subject has any clinical or laboratory abnormalities and is not suitable to participate in this clinical study.

Treatment and study plan

Hemay181

Drug

Hemay181 will be given intravenously on the first day per cycle, and the treatment cycle is 21-days.

Primary outcomes

  1. Number of participants with adverse events

    Time frame: 3 weeks of treatment

  2. Incidence of dose-limiting toxicity (DLT) in each dose group

    Time frame: 3 weeks of treatment

  3. Maximum tolerated dose (MTD) or Maximum climbing dose (MAD) of Hemay181

    Time frame: 3 weeks of treatment

  4. Subsequent recommended doses of Hemay181

    Time frame: 3 weeks of treatment

Secondary outcomes

  1. Objective Response Rate

    Time frame: 3 weeks of treatment

  2. Duration of Response

    Time frame: 3 weeks of treatment

  3. Disease Control Rate

    Time frame: 3 weeks of treatment

  4. Time to Response

    Time frame: 3 weeks of treatment

  5. Progression-Free Survival

    Time frame: 3 weeks of treatment

  6. Maximum Plasma Concentration (Cmax)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  7. Time to reach maximum concentration (Tmax)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  8. Elimination half life(t1/2)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  9. Plasma Clearance(CL)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  10. Mean Residence Time from 0 to last time of quantifiable concentration(MRT 0-t)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  11. Mean Residence Time from 0 to infinite time(MRT 0-∞)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  12. Area under the plasma concentration-time curve from 0 to last time of quantifiable concentration(AUC 0-t)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  13. Area under the plasma concentration-time curve from 0 extrapolated to infinite time(AUC 0-∞)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  14. Percentage of the residual area (AUC%Extra)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  15. Volume of distribution(Vz)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

  16. Elimination rate constant(λz)

    Time frame: 0,0.75, 1.5, 1.75, 2, 2.5, 3.5, 5.5, 9.5, 13.5, 25.5, 49.5, 73.5, 97.5, 121.5 hours post-dose on day 1, and 0,1.5, 2.5 hours post-dose on day 22

    Pharmacokinetic (PK) profile

Study contacts

Contact information is provided by the study sponsor or research team.

Huiping Li

CONTACT

[email protected]

13811012595

Sponsors and collaborators

Lead sponsor

Ganzhou Hemay Pharmaceutical Co., Ltd

Industry

Registry information

Official study title

A Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetic Profile and Preliminary Antitumor Efficacy of Hemay181 in Patients With Advanced Solid Tumors

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Mar 1, 2023
Registry last updated
Apr 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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