Carrimycin in Patients With Locally Advanced Recurrent or Metastatic HNSCC (Non NPC): A Phase I Trial

  • STATUS
    Recruiting
  • participants needed
    9
  • sponsor
    Shanghai Jiao Tong University School of Medicine
Updated on 19 February 2024
platelet count
squamous cell carcinoma of head and neck
squamous cell carcinoma
carcinoma
aptt
metastatic head and neck squamous cell carcinoma
serum total bilirubin
metastatic head and neck squamous cell cancer

Summary

The trial is a study conducted to evaluate the safety, tolerability and PK characteristics of Carrimycin tablet and measure its anti-tumor efficacy initially in the treatment of patients with locally advanced, recurrent, or metastatic head and neck squamous cell carcinoma (non NPC).

Description

This study is a prospective open phase-I study to investigate the safety, tolerability and PK characteristics of Carrimycin tablet in the treatment of patients with locally advanced, recurrent, or metastatic head and neck squamous cell carcinoma (non NPC). The 3x3 dose escalation design will be adopted, including 200mg, 400mg and 600mg of Carrimycin; and three subjects at each dose level initially. If there is no DLT in the dose level of 200mg, the dose level of 400mg will be followed; if there is one DLT in the dose level of 200mg, another three patients will be added in the dose level of 200mg; if there is no DLT occurs in the another three patients, the dose level of 400mg will also be followed; if there is one DLT in the another three patients, the trial will be closed. The same condition to the dose level of 400mg and 600mg. If a patient fails to receive the full prescribed dose for reasons other than DLT at the time of the first administration, the patient will be replaced. Carrimycin treatment to the patients with DLT will be discontinued immediately and they will enter the follow-up period and will not be replaced. The study consists of screening period, treatment period and follow-up period. The treatment period continues until the patients develop progressive disease, dies, lost to follow-up or withdraw informed consent.

Details
Condition Head and Neck Squamous Cell Carcinoma, Oral Squamous Cell Carcinoma
Age 18years - 75years
Treatment Carrimycin
Clinical Study IdentifierNCT04413214
SponsorShanghai Jiao Tong University School of Medicine
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Locally advanced, recurrent, or metastatic head and neck squamous cell carcinoma (non NPC) confirmed by histopathological or cytological diagnosis
Expected life expectancy is no less than 6 months
ECOG PS is 0, 1 or 2
Subjects should be enrolled at least 4 weeks after the lastest treatment of surgery, radiotherapy, chemotherapy, or biotherapy, etc
The laboratory inspection indexes should meet the following requirements: Leukocyte3109/L, Neutrophils1.5109/L, Platelet count75109/LHemoglobin80g/L, Serum total bilirubin1.5ULN, ALT or AST2.5ULN, Creatinine2.0ULN, BUN2.0ULN, Maximum extension of APTT normal is within 10s, Maximum extension of PT normal is within 3s
Women of reproductive age (18-45 years) must have a negative urine pregnancy test and agree to receive effective contraception. Male subjects must voluntarily receive appropriate contraception

Exclusion Criteria

There is still any undiminished CTCAE grade 2 or higher toxicity from previous anti-cancer treatments
There are significant cardiovascular abnormalities (e.g. myocardial infarction, upper-cavity venous syndrome, heart disease of grade 2 or higher diagnosed according to the New York Heart Association (NYHA) classification criteria 3 months prior to enrollment)
There is active severe clinical infection (NCI-CTCAE V5.0 Level 2)
Urine routine shows albuminuria ++, but if albuminuria at baseline ++, patients with albuminuria /24h1g measured quantitatively based on 24-hour urine collection can be enrolled
Allergic to macrolides
Uncontrolled hypertension (systolic > 150 mmHg and / or diastolic >100mmHg) or clinically significant (e.g. active) cardiovascular diseases - such as stroke ( 6 months before randomization), myocardial infarction ( 6 months before randomization), unstable angina pectoris, congestive heart failure of New York Heart Association (NYHA) functional class III or above, or serious arrhythmia that cannot be controlled with drugs or has potential impact on trial treatment
Known to have acute or chronic active HBV or HCV infection and need antiviral treatment with non nucleoside drugs
Women pregnant or lactation
Having participated in other clinical studies and received any other investigational drug for treatment within 30 days before enrollment
Having taken macrolide antibiotics (azithromycin, erythromycin, roxithromycin, clarithromycin, dirithromycin, spiramycin, acetylspiramycin, midecamycin, rokitamycin, meleumycin, josamycin, leucomycin, miocamycin) within 3 days before enrollment
Other cases considered inappropriate by the investigator to participate in the study
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