A Study of BH009 in Head and Neck Squamous Cell Carcinoma and Ovarian Cancer

NCT06232863 | Unknown Phase 1

• 2 other identifiers: BH009-I-101CTR20230004
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 5

Brief Summary

This study will assess the safety and tolerability and pharmacokinetics of BH009 in patients with advanced head and neck squamous (non-nasopharyngeal) and ovarian cancer.

Conditions

Solid Tumor, Adult

Keywords

Phase I

Outcome Measures

Primary Outcomes (3)

• Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

  All adverse events (AE) defined by CTCAE version 5.0

  first dose to 30 days after last dose

• Recommended phase 2 dose of BH009

  defined by CTCAE version 5.0

  first dose to 30 days after last dose

• MTD of BH009

  When the dose is incremented beyond the MTD, the previous lower dose group will be identified as the MTD.

  first dose to 30 days after last dose

Secondary Outcomes (11)

• Objective response rate

  After first dose until 30 days after last dose

• Duration of relief

  After first dose until 30 days after last dose

• Disease control rate

  After first dose until 30 days after last dose

• Progression-free survival

  After first dose until 30 days after last dose

• PK Analysis of BH009

  predose, 30 minutes, 45 minutes, 1 hour after the start of infusion (immediately after the end of infusion), 5 minutes, 15 minutes, 30 minutes, 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours, and 48 hours after the end of infusion

Study Arms (1)

BH009

EXPERIMENTAL

Every 28 days constitutes a treatment cycle, and administration on day 1, day 8, day 15 of each cycle

Drug: BH009

Interventions

BH009 DRUG

Every 28 days constitutes a treatment cycle, and administration on day 1, day 8, day 15 of each cycle

BH009

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female subjects aged between 18-70 years old at the time of informed consent.
• Histologically or cytologically proven squamous cell carcinoma of the head and neck(including oropharynx, oral cavity, hypopharynx and larynx, excluding nasopharyngeal carcinoma) and ovarian carcinoma (including epithelial ovarian carcinoma, fallopian tube carcinoma and primary peritoneal carcinoma).
• Subjects who failed by standard treatments, or refused standard treatments, or the investigator considered the subject unsuitable for standard treatments.
• At least one measurable lesion according to RECIST 1.1 at baseline.
• Subjects must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
• Subjects must have an expected survival of at least 3 months.
• Subjects must have adequate organ and marrow function. Laboratory results meet the following conditions within 7 days prior to the first dose \[subjects must not have received recombinant granulocyte-colony stimulating factor (G-CSF) or blood transfusion within 14 days prior to the first dose\]:
• Hematological : Absolute neutrophil count(ANC)≥1.5×109/L, platelet count(PLT)≥100×109/L, hemoglobin(Hb)≥90 g/L;
• Renal function :Serum creatinine(Cr)≤1.5×ULN and creatinine Clearance ≥50 mL/min(Cockcroft-Gault );
• Liver function : Total bilirubin ≤1.5×ULN, alanine aminotransferase(ALT)and aspartate aminotransferase(AST) ≤ 1.5×ULN (if liver tumor/metastases are present, then ≤2.5×ULN is allowed).
• Subjects with a left ventricular ejection fraction of ≥50% measured by echocardiography at baseline, a normal 12-lead electrocardiogram or no clinically significant abnormalities, QTc intervals \<450 ms (men) or \<470 ms (women) (Fridericia's), and no signs or symptoms of heart failure.
• Subjects with remission of toxicity due to prior therapy to ≤ grade 1 (except for toxicities such as alopecia that are not considered a safety risk by investigator).
• Subjects have not received surgery, chemotherapy, radiotherapy, immunotherapy, biotherapy, targeted therapy, anti-tumour herbs, small molecule targeted drugs, within 4 weeks or 5 half-lives (whichever is shorter) prior to the first dose of the drug.
• Subjects voluntarily signed the informed consent form, had good compliance, were available for follow-up, and voluntarily complied with study regulations.

You may not qualify if:

• Subjects with a known hypersensitivity to the study drug and any excipient contained in the drug formulation,or intolerance to paclitaxel analogues.
• Subjects are currently receiving other anti-tumor therapy.
• Subjects requiring a potent inhibitor of CYP3A4 within 14 days prior to the first dose and during the study period.
• Subjects have been treated with systemically administered glucocorticosteroid (prednisone \> 10 mg/day or equivalent dose of other similar drug) or other immunosuppressive agents within 14 days prior to the first use of the investigational medicinal product; with the exception of the following: treatment with topical, ophthalmic, intra-articular, intranasal, and inhaled glucocorticosteroids; and short-term prophylactic glucocorticosteroids (e.g., prevention of allergy to contrast media).
• Subjects with clinically significant psychiatric or central nervous system disorders.
• Subjects with a primary malignant tumour of the brain; or those who with two or more malignant tumours (except cured non-melanoma skin cancer, cervical cancer, thyroid cancer and intramucosal cancer of the gastrointestinal tract).
• Subjects who with serious medical conditions:
• Subjects with clinically significant cardiovascular disease, including: severe or uncontrolled heart disease requiring treatment, congestive heart failure classified by the New York Heart Association (NYHA) as grade 3 or 4, unstable angina pectoris uncontrolled by medication, history of myocardial infarction within 6 months prior to enrolment, severe arrhythmia requiring medication (except atrial fibrillation or paroxysmal supraventricular tachycardia);
• Subjects with indwelling cardiac stents within 6 months;
• Subjects with uncontrolled hypertension (systolic blood pressure ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg after pharmacological intervention), diabetes mellitus (glycated haemoglobin HbA1c ≥8.0% or fasting blood glucose ≥10.0 mmol/L), pleural effusion, pericardial effusion, ascites;
• Subjects have uncontrolled peptic ulcer, or other uncontrolled thromboembolic event;
• Subjects with interstitial lung disease, pulmonary fibrosis, or a history of pneumonia requiring steroid therapy.
• Subjects with known HIV, HBV, HCV, and syphilis spirochete infections (hepatitis B surface antigen (HBsAg)-positive with HBV-DNA greater than 1,000 IU/mL; HCV-Ab-positive with a copy number higher than the upper limit of normal on the HCV RNA assay); and uncontrolled active infections (in those requiring systemic anti-infective therapy, or subjects with a temperature of \>38°C (axillary temperature) prior to dosing and unable to explain it).
• Subjects have a history of drug abuse.
• Pregnant or nursing women; positive pregnancy test within 7 days prior to the first dose in female subjects of childbearing potential; any female subjects of childbearing potential does not consent to use of a medically recognised effective method of contraception throughout the trial period and for 3 months after the the last dose.

Sponsors & Collaborators

• Zhuhai Beihai Biotech Co., Ltd: lead

Study Sites (5)

The First Affiliated Hospital of Bengbu Medical University

Bengbu, Anhui, China

RECRUITING

The First Affiliated Hospital, Sun Yat-sen University

Guangzhou, Guangdong, China

RECRUITING

Hunan Cancer Hospital

Changsha, Hunan, China

RECRUITING

Affiliated Zhongshan Hospital Of Dalian University

Dalian, Liaoning, China

RECRUITING

Obstetrics & Gynecology Hospital of Fudan University

Shanghai, Shanghai Municipality, China

RECRUITING

Study Officials

• Jing Wang, PI

  Hunan Cancer Hospital

  PRINCIPAL INVESTIGATOR

• Yaqian Han, PI

  Hunan Cancer Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Xiaohua Wei, PM

CONTACT

13500248359; xhwei@bayhibiotech.com

Mingyue Zeng, APM

CONTACT

15113340590; myzeng@bayhibiotech.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 19, 2024
• First Posted: January 31, 2024
• Study Start: January 18, 2023
• Primary Completion: March 30, 2024
• Study Completion: April 30, 2024
• Last Updated: February 2, 2024

Record last verified: 2024-01

Data Sharing

• IPD Sharing: Will not share

Locations

CN (5)