Technetium [99mTc]-H7ND in Patients With Gastrointestinal Malignancies and Healthy Volunteers

Solid Tumor Clinical Trial

Official title:

A Phase I Clinical Study of the Pharmacokinetics and Safety of Technetium [99mTc]-H7ND Injection in Patients With Gastrointestinal Malignancies and Healthy Volunteers

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06443710
• Other study ID #: 2023LP02630
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: May 30, 2024
• Est. completion date: December 31, 2024

Study information

• Verified date: May 2024
• Source: Jiaxing Pharmadax Genesis Pharmaceutical Technology Co.,Ltd.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is: to evaluate the safety of technetium [99mTc]-H7ND injection in patients with gastrointestinal malignancies and in healthy subjects. The secondary objectives of this study are: (1) to examine the pharmacokinetics of technetium [99mTc]-H7ND Injection in healthy subjects. (2) Detect the metabolic stability of technetium [99mTc]-H7ND injection in healthy humans. (3) Detect the biodistribution and estimate the absorbed dose of radiation from internal irradiation of technetium [99mTc]-H7ND injection in patients with malignant tumors of the gastrointestinal tract and in healthy humans.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 24
• Est. completion date: December 31, 2024
• Est. primary completion date: December 31, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. All subjects should be adult males or females aged 18-75 years (including borderline values, based on the time of signing the informed consent form) at screening, and not less than 1/3 of the total number of cases of each gender

2. All subjects who are males or females of childbearing potential must be using effective contraception during the study period (effective contraception means sterilization, intrauterine hormonal devices, condoms, contraceptive pills/agents, abstinence, or vasectomy)

3. All subjects are fully aware of the purpose, nature, methods, and possible adverse effects of the trial, voluntarily participate and sign a written informed consent form, and are able to follow the protocol requirements to complete the study

4. Healthy subjects with a body mass index within the range of 18.0 to 26.0 kg/m2 (including the borderline value), male subjects weighing = 50 kg, female subjects weighing = 45 kg

5. Healthy subjects are in good health or do not have a history of major diseases

6. Vital signs, physical examination, laboratory tests, and 12-lead electrocardiogram (ECG) results of healthy subjects during the screening period are not abnormal or the abnormalities are not clinically significant.

7. Gastrointestinal malignant tumor subjects with histologically/cytologically confirmed diagnosis of gastrointestinal malignant tumors (including stomach, small intestine and colorectum)

8. Subjects with gastrointestinal malignant tumors with an ECOG score of 0 - 1

9. Subjects with gastrointestinal malignant tumors Blood routine: WBC = 3 × 109 / L, ANC = 1.5 × 109 / L, Hb = 90 g / L, PLT = 75 × 109 / L; Liver function: TBIL = 1.5 × ULN, ALT, AST = 3 × ULN (= 5 × ULN for liver metastases); Kidney function: Cr = 1.5 × ULN; Coagulation function: Prothrombin time (PT) =1.5×ULN, activated partial thromboplastin time (APTT) =1.5×ULN, international normalized ratio (INR) =1.5×ULN; Electrolytes: corrected magnesium =LLN, allowed to correct electrolytes during the screening period Cardiac function: left ventricular ejection fraction = 50%

10. Subjects who have recovered to Grade 1 (CTCAE Version 5.0) from damage caused by other therapies, except: alopecia, hyperpigmentation; and if nutritionally stable, the presence of irrecoverable long-term toxicity as determined by the Investigator is permitted.

11. Subjects with gastrointestinal malignancies expected to survive = 12 weeks

Exclusion Criteria:

1. Pregnant (positive screening pregnancy test) or breastfeeding female

2. History of alcohol or drug abuse/dependence

3. Known allergy to radioactive rays, or history of other severe allergies

4. Human immunodeficiency virus (HIV) positive or not definitively negative, hepatitis C virus (HCV) or syphilis spirochete antibody test positive, hepatitis B virus (HBV) surface antigen positive and quantitative HBV DNA test = 1.0×103 IU/mL

5. Significant occupational exposure to ionizing radiation in the past 10 years

6. Unable to repeat venipuncture

7. Participation in a clinical study of another drug within 30 days prior to screening and use of another test drug

8. Other conditions that, in the opinion of the investigator, make participation in this clinical trial inappropriate

9. Subjects with gastrointestinal malignancies requiring treatment of symptomatic brain metastases

10. Subjects with gastrointestinal malignancies who have a history of other malignancies, except for malignant lesions that have been treated with therapeutic measures 5 or more years prior to the initiation of investigational drug use and are not known to be active, and who, in the judgment of the Investigator, are at low risk of recurrence. Adequately treated non-melanoma skin cancer or malignant freckle-like nevus without evidence of disease progression. Adequately treated in situ cervical cancer with no evidence of progression. Intraepithelial tumor of the prostate gland without evidence of prostate adenocarcinoma

11. Subjects with gastrointestinal malignancies who have developed clinically significant cardiovascular disease (including, but not limited to, myocardial infarction, unstable angina pectoris, symptomatic congestive heart failure, and uncontrolled severe arrhythmia) within 6 months prior to initiation of study drug use

12. Subjects with gastrointestinal malignancies who have hypertension that is uncontrollable with a single agent

13. Subjects with malignant tumors of the gastrointestinal tract who have a history of hepatic disease or other conditions that interfere with the absorption, distribution, excretion, or metabolism of the drug, as determined by the investigator

14. Subjects with gastrointestinal malignancies have a history of coagulopathy or coagulation disorders.

15. History of arterial or venous embolism in subjects with gastrointestinal malignancies

16. Subjects with gastrointestinal malignancies who, in the judgment of the investigator, have received any medications and treatments prior to enrollment that may interfere with the trial data or that may have resulted in serious side effects that have not been fully cleared

17. Subjects with gastrointestinal malignancies who have an active or uncontrolled infection requiring systemic therapy within 14 days prior to initiation of study drug use

18. Subjects with malignant tumors of the gastrointestinal tract who have undergone major surgical procedures within 28 days prior to the start of investigational drug use-

Related Conditions & MeSH terms

• Neoplasms
• Solid Tumor

Intervention

Drug:
• Technetium [99mTc]-H7ND injection
Technetium [99mTc]-H7ND injection is a radiolabeled fibroblast activation protein inhibitor

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Jiaxing Pharmadax Genesis Pharmaceutical Technology Co.,Ltd.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Security Indicators	Evaluation of adverse events and serious adverse events according to the Common Terminology Criteria for the Evaluation of Adverse Events (NCI-CTCAE) version 5.0	1-7 days from time of injection
Secondary	uptake value ratio	Measure the count ratio of technetium [99mTc]-H7ND tumor area to blood pool, surrounding normal tissue, liver, and muscle in the integrated region of interest.	3 days after injection
Secondary	biodiversity distribution	SPECT/CT whole-body scans were performed at different time points after drug injection to obtain radioactivity counts (%ID) in each major irradiated organ at each time phase to reflect the biodistribution of the drug in the body	3 days after injection
Secondary	internal radiation dose	Plot the "time-activity count" curve for each major organ and calculate the area under the curve. Calculate the retention time of each major exposed organ and apply the software to estimate the absorbed dose of internal radiation for each major exposed organ.	3 days after injection
Secondary	Concentration of technetium [99mTc] H7ND prototype and its radioactive metabolites	Blood samples were collected at different time points after drug injection, and urine samples were collected at different time intervals for detection of technetium [99mTc] H7ND prototype and its radioactive metabolites using either a radioactive HPLC detector or a radioactive TLC detector.	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	Cmax	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	AUC(0-t)	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	AUC(0-8)	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	Tmax	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	T1/2	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	AUC_%Extrap	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	CL	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	Vd	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	MRT	Predose and up to 72 hours postdose
Secondary	Pharmacokinetic parameters	?z	Predose and up to 72 hours postdose