Search / Trial NCT06223308

A Study Evaluating the Safety and Efficacy of HB0028 in Subjects With Advanced Solid Tumors

Launched by SHANGHAI HUAOTA BIOPHARMACEUTICAL CO., LTD. · Jan 15, 2024

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Trial Information

Current as of December 21, 2024

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called HB0028 for patients with advanced solid tumors, particularly focusing on cervical cancer. The goal is to find out how safe the treatment is and whether it works effectively for patients whose previous cancer treatments haven’t helped. The trial is currently looking for participants who are at least 18 years old and have specific types of advanced cancer that are no longer responding to standard therapies. Eligible patients should also have a measurable tumor that can be assessed by imaging tests and meet certain health criteria.

If you or someone you know qualifies for this study, participants can expect to receive the study drug and be closely monitored for any side effects or results from the treatment. The trial is taking place at multiple centers, and all genders are welcome to participate. It’s important for potential participants to understand the requirements for joining and to discuss any concerns with their healthcare provider before enrolling. This trial represents an opportunity to explore a potential new treatment option for those with limited choices left.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • * Patients must meet all the following criteria to be eligible for participation in this study:
  • • 1. Male or female. Age ≥ 18 years.
  • • 2. The subject is able to understand and willing to sign the Informed Consent Form(ICF); willing and able to comply with all study procedures.
  • • 3. a) dose escalation: Patients with histologically or cytologically confirmed locally advanced, recurrent, or metastatic solid tumors (or clinically diagnosed hepatocellular carcinoma) that failed all standard therapies known to provide clinical benefit; \[These solid tumors include but not limit to: non-small cell lung cancer, esophageal squamous cell carcinoma, melanoma, head and neck squamous cell carcinomas, hepatocellular carcinoma, gastric or gastroesophageal junction adenocarcinoma, renal cell carcinoma, etc.\].
  • • b) dose expansion (Cervical cancer group): Histologically confirmed persistent, recurrent, or metastatic (\[International Federation of Gynecology and Obstetrics(FIGO)\] stage IVB) cervical cancer that is not eligible for curative surgery and/or definitive concurrent radiotherapy; The pathological type was squamous cell carcinoma, adenocarcinoma or adenosquamous carcinoma.; According to the investigator's judgment, it may benefit from the study drug treatment; patients with disease progression after at least one previous systemic therapy (such as systemic chemotherapy).
  • • 4. At least one measurable tumor lesion was present according to RECIST 1.1. A baseline imaging assessment could be performed up to 28 days before the first dose.
  • • 5. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1.
  • • 6. Life expectancy ≥12 weeks
  • 7. liver function requirements:
  • • 1. Total bilirubin (TBIL) ≤ 1.5×ULN
  • • 2. Aspartate aminotransferase(AST) and Alanine aminotransferase(ALT) ≤ 2.5×ULN; AST or ALT ≤5×ULN if liver metastases are present;
  • • 8. Creatinine (Scr) \< 1.5×ULN and Calculated creatinine clearance (CrCL) \> 50 mL/ min (Cockroft-Gault Equation);
  • • 9. Hematology absolute neutrophil count (ANC) ≥ 1.5×109/L; hemoglobin (HGB) ≥ 90 g/L ；platelets (PLT) ≥ 75×109/L;
  • • 10. Coagulation function: International Normalized Ratio(INR)≤ 1.5×ULN; Prothrombin Time(PT)≤ 1.5×ULN; Activated Partial Thromboplastin Time(APTT)≤ 1.5×ULN. No active or clinically significant bleeding within 14 days before the first dose.
  • • 11. Recovery to Grade 0-1 from adverse events (AEs) related to prior anticancer therapy except alopecia, \< Grade 2 sensory neuropathy, and endocrinopathies controlled with hormone replacement therapy
  • • 12. Women of childbearing potential must confirm a negative serum or urine pregnancy test within 3 days prior to the initiation of study treatment; Fertile patients and their partners must agree to use effective contraceptives for the duration of study drug use and for 90 days after the last administration of study treatment.
  • Exclusion Criteria:
  • * Exclusion Criteria Patients are excluded from the study if any of the following criteria apply:
  • • 1. Have clinically active central nervous system (CNS) metastases. Patients with previously-treated brain or meningeal metastases may participate and be eligible for treatment provided they are stable (\>4 weeks) and asymptomatic. Patients with asymptomatic brain metastasis or subjects who are symptomatically stable after treatment and are on \< 10 mg/d prednisone or equivalent are eligible.
  • • 2. dose expansion (Cervical cancer group): Hydronephrosis, which could not be relieved by clinical treatment
  • • 3. Active autoimmune disease or history of autoimmune disease requiring systemic therapy \< 2 years prior to screening except hypothyroidism, vitiligo, Grave's disease, Hashimoto's disease, or Type I diabetes. Patients with childhood asthma or atopy that has not been active in the 2 years prior to study screening are eligible.
  • • 4. History of Grade 3-4 immune-related adverse events (irAEs) or irAEs requiring discontinuation of prior therapies, (except for grade 3 endocrinopathy that is managed with hormone replacement therapy).
  • • 5. Use of systemic corticosteroids in a dose equivalent to \>10 mg/day of prednisone or other immunosuppressive agent \< 2 weeks prior to screening; the use of topical, intraocular, intraarticular, intranasal, or inhaled corticosteroids and systemic steroids to prevent (e.g., allergy to contrast agents) or treat non-autoimmune condition (e.g., delayed hypersensitivity caused by exposure to allergens) or short course (\< 5 days) will be allowed
  • • 6. Cerebrovascular accident (CVA), transient ischemic attack (TIA), myocardial infarction (MI), unstable angina, or New York Heart Association (NYHA) class III or IV heart failure \< 6 months of study entry; uncontrolled arrhythmia \< 3 months of study entry; mean ECG QT-interval corrected according to Fridericia's formula (QTcF) \> 470 milliseconds (ms) obtained from three ECGs;
  • • 7. uncontrolled diabetes, glycosylated hemoglobin HbA1c \>8%；
  • • 8. Anticancer therapy or radiation \< 5 half-lives or 4 weeks (whichever is shorter) prior to study entry; palliative radiotherapy to a single area \< 2 weeks prior to study screening is permitted. Measurable lesions cannot be previously irradiated unless they have demonstrated growth after radiation therapy (According to RECIST v1.1).
  • • 9. Patients who have previously received allogeneic stem cell, Bone marrow or solid organ transplantation.
  • • 10. The following infections are present
  • • 1. Active infection requiring intravenous treatment within 2 weeks before screening
  • • 2. Active Pulmonary tuberculosis
  • • 3. Positive results for HIV test
  • • 4. Active hepatitis B or C. Patients with asymptomatic hepatitis B virus carriers (HBV DNA titer \< 1000 cps/mL or 200 IU/mL) or cured hepatitis C virus(HCV)(negative HCV RNA test) may be enrolled;
  • • 11. Major surgery \< 4 weeks prior to the first dose; Minor surgery \< 2 weeks prior to the first dose
  • • 12. History of severe allergic reactions, grade 3-4 allergic reactions to treatment with another monoclonal antibody, or known to be allergic to protein drugs or recombinant proteins or excipients in HB0028 drug formulation;
  • • 13. Have received or will receive a live vaccine within 30 days prior to the screening.
  • • 14. Patients who have participated in any clinical trial of a drug or medical device within 30 days prior to the first dose
  • • 15. Any other serious underlying medical condition (e.g., active gastric ulcer, uncontrolled seizures, cerebrovascular incidents, gastrointestinal bleeding, severe signs and symptoms of coagulation and clotting disorders, cardiac conditions), or psychiatric, psychological, familial condition or geographical location that, in the judgment of the Investigator, may interfere with the planned staging, treatment and follow-up, affect patient compliance or place the patient at high risk from treatment.
  • • 16. Positive COVID-19 quantitative real time (qRT) polymerase chain reaction (PCR) or rapid screening test during screening;
  • • 17. Patients with a history of arterial or deep vein thrombosis within 6 months before enrollment; evidence or history of a bleeding tendency within 2 months before enrollment
  • • 18. Severe dyspnea, pulmonary insufficiency or the need for continuous supportive oxygen therapy
  • • 19. The surgical site, the wound site, the mucous membrane severely ulcerated, or the fracture did not heal completely
  • • 20. Conditions that may cause bleeding or perforation of the digestive tract (such as duodenal ulcer, intestinal obstruction, Crohn's disease, Ulcerative colitis, large gastrectomy and small bowel resection, etc.); Patients with a history of intestinal perforation and fistula, who were not cured after surgical treatment; Esophageal and gastric varices
  • • 21. Immunomodulatory therapy was administered within 2 weeks before enrollment (including but not limited to cyclosporine and tacrolimus)
  • • 22. Have history of interstitial lung disease or non-infectious pneumonitis, except from radiotherapy (the enrollment of subjects needs to be considered after discussion with MM);
  • • 23. Other conditions which would make it inappropriate for the patient to participate as judged by the investigator.

Trial Officials

Jing Wang, MD/PHD

Principal Investigator

Hunan Cancer Hospital

About Shanghai Huaota Biopharmaceutical Co., Ltd.

Shanghai Huaota Biopharmaceutical Co., Ltd. is a leading biopharmaceutical company based in Shanghai, specializing in the research, development, and commercialization of innovative therapeutics. Committed to advancing healthcare, Huaota focuses on harnessing cutting-edge biotechnologies to address unmet medical needs across various therapeutic areas, including oncology, autoimmune diseases, and infectious diseases. With a robust pipeline of clinical trials, the company aims to deliver high-quality, effective treatment options while adhering to stringent regulatory standards and fostering collaborations within the global biopharmaceutical community.

Locations

Changsha, Hunan, China

Changsha, Hunan, China

Changsha, Hunan, China

People applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0