Trial Title:
CTS2190 Phase I /II Clinical Study in Patients
NCT ID:
NCT06224387
Condition:
Solid Tumors
Pancreatic Cancer
Non-small Cell Lung Cancer
Triple-negative Breast Cancer
Conditions: Official terms:
Triple Negative Breast Neoplasms
Conditions: Keywords:
Phase I/II
pharmacodynamic
Pharmacokinetics
Tolerability
Study type:
Interventional
Study phase:
Phase 1/Phase 2
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Intervention model description:
QD and durg holiday,PO.
Primary purpose:
Treatment
Masking:
None (Open Label)
Masking description:
QD and durg holiday,PO.
Intervention:
Intervention type:
Drug
Intervention name:
CTS2190 capsules
Description:
4-6 dose groups are pre-specified in Dose Escalation,and 4 arms in Dose Expansion.
Arm group label:
Dose Escalation/Dose Expansion
Other name:
CTS2190
Summary:
This is a first in human study in patients with advanced or metastatic solid tumors. The
first part of the study is an open-label, dose escalation and the second part is an open
label dose expansion in specific tumor types. The study drug, CTS2190, is a PRMT1
inhibitor administered orally. The study is planned to treat up to 224 participants.
Detailed description:
This is a Phase 1/2 multi-center, open label study in solid tumor patients. Phase
1（Part1) is a dose escalation study of oral CTS2190 in patients with solid tumors，which
is planned to treat up to 144 participants.
Phase 2（Part2) is an open label, dose expansion study in specific tumor types. In both
parts of the study, participants who tolerate the drug may continue the treatment until
disease progression.
The study duration for each subject is defined as beginning from 28 days prior to the
first dose, until the subject withdrawal of informed consent, end of treatment, loss to
follow-up or death, completes 48 weeks of continuous treatment or the study ends early,
whichever occurs first. The end of study is defined as the date when the last subject
completes the last visit specified in the protocol.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
Subjects who meet all of the following criteria can be included in this study:
1. Male or female ≥ 18 years of age at signing of ICF.
2. Part 1: histologically or cytologically confirmed locally advanced or metastatic
solid tumors at screening who cannot be treated surgically and have failed standard
treatment (PD during treatment or after the last treatment) recommended by the
current clinical diagnosis and treatment standards or guidelines, or cannot tolerate
standard treatment, or refuse standard treatment and/or currently have no effective
treatment available.
Part 2: histologically or cytologically confirmed advanced solid tumors (including
pancreatic cancer, non-small cell lung cancer and/or other tumors, such as gastric
cancer, colorectal cancer, etc.) at screening who cannot be treated surgically and
have failed standard treatment (PD during treatment or after the last treatment)
recommended by the current clinical diagnosis and treatment standards or guidelines,
or cannot tolerate standard treatment, or refuse standard treatment and/or currently
have no effective standard treatment available.
3. At least one measurable tumor lesion at screening [according to RECIST V1.1 criteria
(see appendix 1)].
4. Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1 (Appendix 2) at
screening.
5. With a life expectancy ≥ 12 weeks at screening.
6. With good organ function at screening, including:
- Liver function: total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN) (if
the following conditions occur, isolated bilirubin >1.5 × ULN is acceptable if:
bilirubin is fractionated and direct bilirubin <35%, or the patients is
diagnosed with Gilbert syndrome), alanine aminotransferase (ALT) ≤ 2.5 × ULN,
and aspartate aminotransferase (AST) ≤ 2.5 × ULN (for patients with liver
metastases or tumor infiltration, the criteria can be relaxed to TBIL ≤ 1.5 ×
ULN, ALT ≤5 × ULN, and AST ≤ 5 × ULN);
- Renal function: blood creatinine ≤ 1.5 × ULN and creatinine clearance ≥ 50
mL/min [calculate the creatinine clearance using Cockcroft-Gault formula
(appendix 3)];
- Hematology: platelet ≥ the lower limit of the laboratory normal range, and
absolute neutrophil count (ANC) ≥ 1.5 × 109/L, and hemoglobin ≥ 100 g/dL;
- Cardiac function: QT interval corrected by Fridericia method (QTcF) ≤ 450 ms
(male) or ≤ 470 ms (female) (see the appendix 3 for calculation formula).
- Coagulation function: International normalized ratio (INR) ≤ 1.5 × ULN, or
activated partial thromboplastin time (APTT) ≤ 1.5 × ULN.
7. Female patients of non-childbearing age or female patients of childbearing age who
have negative pregnancy test results and promise to take sufficient and effective
contraceptive measures or adhere to abstinence from the screening period to 90 days
after the last administration, or male patients who promise to take sufficient and
effective contraceptive measures or adhere to abstinence from the screening period
to 90 days after the last administration (see the appendix 4). Patients are not
allowed to donate sperm within 6 months from the start of administration to 6 months
after the end of investigational drug administration.
8. Patients who understand and voluntarily signs the ICF, are willing to and able to
complete the scheduled visits, treatment plan, laboratory tests and other study
procedures.
Exclusion Criteria:
Subjects should not participate in this clinical study if any of the following conditions
is met:
1. Female patients in pregnancy or lactation.
2. Patients with dysphagia.
3. Patients who cannot tolerate venipuncture or have a history of syncope judged by the
investigator to be clinically significant.
4. Uncontrolled tumor-related pain.
5. Allergic or intolerant to the active ingredients or excipients of the
investigational drug judged by the investigator.
6. Treatment with radiotherapy for the target lesion within 4 weeks before the first
administration of the investigational drug, or accepted any anti-tumor drugs/
treatments (including but not limited to chemotherapy, targeted therapy,
immunotherapy) within 5 half-lives before the first administration of the
investigational drug, whichever is longer; or patients who have received herbal
therapies with anti-tumor indications within 1 week before the first administration.
7. Primary central nervous system (CNS) tumor or CNS metastasis at screening. The
following patients can be considered for enrollment: after treatment and being
stable for ≥ 3 months, patients who have completed the treatment at least 10 days
before the start of the study treatment; the corticosteroid treatment has been
terminated for ≥ 5 days when the study treatment starts, the neurological function
is stable, and it is estimated that no steroids or antiepileptic drugs will be
required during the study treatment.
8. Patients judged by the investigator to have uncontrolled pleural effusion,
pericardial effusion, or peritoneal effusion (requiring repeated drainage, multiple
times a month or more frequently) at screening. Allow patients to indwell catheters
regardless of drainage frequency.
9. Patients with untreated or clinically symptomatic spinal cord compression that has
not been controlled (except for patients who have received treatment and have stable
symptoms, whose imaging examination shows that they are stable for at least 4 weeks
before the first administration, and who have no evidence of brain edema and do not
require glucocorticoid treatment).
10. Patients with ≥ 2 malignant tumors within 5 years before the first administration.
Except for cured early-stage malignancies (carcinoma in situ or stage I tumor), such
as adequately treated cervical carcinoma in situ, basal cell or squamous epithelial
cell skin cancer.
11. Patients who are found to have active pulmonary tuberculosis infection within 1 year
before enrollment through medical history, or those with a history of active
pulmonary tuberculosis infection more than one year ago who have not received formal
treatment.
12. Interstitial lung disease or interstitial pneumonia, including clinically
significant radiation pneumonia (i.e., affecting activities of daily living or
requiring intervention).
13. Severe infection within 4 weeks before the first administration, including but not
limited to bacteremia and severe pneumonia, etc. requiring hospitalization; CTCAE ≥
grade 2 active infection requiring systemic antibiotic treatment within 2 weeks
before the first administration.
14. History of serious cardiovascular and cerebrovascular diseases, including but not
limited to serious cardiac rhythm or conduction abnormalities, such as ventricular
arrhythmia requiring clinical intervention, degree II-III atrioventricular block,
etc.; acute coronary syndrome, congestive cardiac failure, aortic dissection, stroke
or other grade 3 or above cardiovascular and cerebrovascular events within 6 months
before the first administration; New York Heart Association (NYHA) cardiac function
classification (see appendix 5) ≥ grade II or left ventricular ejection fraction
(LVEF)<50% or hypertension that cannot be clinically controlled (systolic blood
pressure ≥ 150 mmHg, diastolic blood pressure ≥ 100 mmHg).
15. Positive hepatitis B virus surface antigen (HBsAg) and the number of copies of
hepatitis B virus (HBV) deoxyribonucleic acid (DNA) ≥ 500 IU/mL (or 2500 copies, or
the lower limit of the positive detection value of the study site) at screening,
HBsAg (-), hepatitis B core antibody (HBcAb) (+) and the number of copies of HBV
DNA≥ 500 IU/mL (or 2500 copies, or the lower limit of the positive detection value
of the study site) after treatment of HBV infection, or positive hepatitis C
antibody (HCVAb) and hepatitis C virus (HCV) ribonucleic acid (RNA) ≥ ULN of the
study site; those with a history of liver cirrhosis (Child Pugh class B or C) or
active syphilis infection.
16. Patients who have active diseases or a history of autoimmune diseases that may
relapse (such as systemic lupus erythematosus, rheumatoid arthritis, vasculitis,
etc.) at screening, except patients suffering clinically stable autoimmune thyroid
disorder.
17. History of immunodeficiency, including HIV positive, or those suffering from other
acquired or congenital immunodeficiency diseases, or with a history of allograft.
Autotransplantation should be completed at least 3 months before screening.
18. Those who had clinically significant hemorrhage symptoms within 3 months before the
first administration. Patients who significantly coughed up blood within 4 weeks
before the first administration of the investigational drug, and the amount of
hemoptysis each time reached half a teaspoon (2.5 mL) or more; patients who had
arterial/venous thrombosis events within 6 months before the first administration,
such as cerebrovascular accident, deep vein thrombosis and pulmonary embolism,
central retinal vein occlusion (RVO), etc.; those who are receiving anticoagulant
treatment at the time of screening; patients with potential thrombosis or at the
risk of coagulation judged by the investigator.
19. Patients who have received other unlisted clinical investigational drugs or
treatments within 4 weeks (or 5 drug half-lives, whichever is longer) before the
first administration.
20. Patients who have used live vaccine or attenuated vaccine within 4 weeks before the
first administration, or plan to use live vaccine or attenuated vaccine during the
study period.
21. Patients who have used potent cytochrome enzyme (CYP)3A4 inhibitors or inducers
within 2 weeks before the first administration, or need to use potent CYP3A4
inhibitors or inducers until 7 days after the last dose (see the appendix 6).
22. Major surgery (except for surgery for diagnostic purposes) within 4 weeks before the
first administration, or expected to undergo major surgery (except for surgery for
diagnostic purposes) during the study period, or have undergone diagnostic or
minimally invasive surgery within 7 days before the first administration.
23. Adverse reactions from previous anti-tumor treatment have not recovered to ≤ CTCAE
V5.0 grade 1 (except for alopecia and grade 2 neurotoxicity caused by chemotherapy
drugs, grade 2 hypothyroidism caused by anti-tumor treatments, hypertension and
other toxicities that are judged to have no safety risks by the investigator).
24. Patients who are judged by the investigator to have a history of other serious
systemic diseases, or not suitable for participating in the trial for any other
reason (the patient has mental illness, alcohol abuse, drug use or drug abuse that
may affect his/her compliance with the trial or may interfere with the
interpretation of the study results).
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
The First Affiliated Hospital of Henan University of Science and Technology
Address:
City:
Luoyang
Zip:
471000
Country:
China
Status:
Recruiting
Contact:
Last name:
yao J, Doctor
Phone:
136 6379 0098
Email:
yaojun74@163.com
Contact backup:
Last name:
yang J Q, Doctor
Facility:
Name:
Zhejiang Cancer Hospital
Address:
City:
Hangzhou
Zip:
310022
Country:
China
Status:
Recruiting
Contact:
Last name:
Cheng X Dong, PHD
Phone:
13968032995
Phone ext:
86-10
Email:
Chengxd516@126.com
Contact backup:
Last name:
Song Z Bo, PHD
Phone:
13857153345
Phone ext:
86-10
Email:
songzb@zjcc.org.cn
Start date:
June 26, 2023
Completion date:
October 31, 2025
Lead sponsor:
Agency:
CytosinLab Therapeutics Co., Ltd.
Agency class:
Industry
Source:
CytosinLab Therapeutics Co., Ltd.
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06224387
