OH2 Injection in Solid Tumors

  • STATUS
    Recruiting
  • days left to enroll
    76
  • participants needed
    30
  • sponsor
    Wuhan Binhui Biotechnology Co., Ltd.
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Updated on 27 April 2022
See if I qualify
cancer
measurable disease
breast cancer
colony stimulating factor
metastasis
liver metastasis
mitomycin
solid tumour
targeted therapy
sarcoma

Summary

This phase I study evaluates the safety and efficacy of OH2 as single agent or in combination with Keytruda, an anti-PD-1 antibody, in patients with malignant solid tumors (Melanoma).

OH2 is an oncolytic virus developed upon genetic modifications of the herpes simplex virus type 2 strain HG52, allowing the virus to selectively replicate in tumors. Meanwhile, the delivery of the gene encoding human granulocyte macrophage colony-stimulating factor (GM-CSF) may induce a more potent antitumor immune response.

Details
Condition Solid Tumor, Melanoma
Treatment Keytruda, OH2 injection
Clinical Study IdentifierNCT04386967
SponsorWuhan Binhui Biotechnology Co., Ltd.
Last Modified on27 April 2022

Eligibility

 Yes No Not Sure

Inclusion Criteria

The non-operative stage III or stage IV malignant tumor patients with clear diagnosis by pathology and/ or cytology; breast cancer, gastrointestinal adenocarcinoma, liver cancer, cervical cancer, malignant melanoma, head and neck tumors, Priority inclusion in soft tissue sarcomas (mainly for melanoma patients at the dose extension phase)
The absence of a conventional effective treatment or treatment failure or recurrence by a conventional method
Male or female patients, aged 18 ≤ 75 years (including boundary value), general physical condition score ECOG 0 ≤ 1, expected survival time more than 3 months
Prior anti-tumor treatment (including endocrine, chemical/ radiotherapy,targeted therapy) was over 4 weeks (more than 6 weeks of discontinuation using nitroso-and mitomycin-based chemotherapy) and was recovered to grade 1 from the side effects of prior treatment
Those who have undergone major surgery will have to undergo surgery for four weeks
There is at least one measurable lesion that is suitable for intratumoral injection. According to RECIST version 1.1, it is determined that at least once the CT or MRI examination shows the tumor lesion, it is possible to measure the tumor focus. The measured tumor focus is defined as the longest diameter ≥ 10 mm and the scanning thickness is not more than 5.0 mm. For lymph node lesions, the short diameter is ≥ 15 mm
There is no serious dysfunction of the main organs
(a) WBC≥3.0×109／L，ANC≥2.0×109／L ，PLT≥100×109／L，Hb≥90 g/L； (b) BUN and Scr. were in the upper limit of 1.5 times of the normal value; (c) TBIL≤ 1.5 times the upper limit of the normal value. (d) ALT and AST ≤ 2.5 times the upper limit of normal value; The value of patients with liver metastasis did not exceed 5 times the upper limit of normal value. (e) Coagulation function is normal (PT and APPT are within 1.5 times of the upper limit of normal value)
Female subjects and their spouses received effective contraceptives during and within 3 months of treatment
Subjects with herpes in the reproductive organs needed three months after the end of herpes
The informed consent was voluntarily signed and the expected compliance was good

Exclusion Criteria

Severe medical diseases, including severe heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hypertension, severe infection, active digestive tract ulcer, abnormal immune function (including, but not limited to, rheumatoid arthritis, lupus erythematosus, Sjogren's syndrome, etc.)
History of primary grape-film melanoma or other malignant tumors in the 3 years prior to treatment. (use of combination drugs only)
Past or present immunodeficiency diseases. (use of combination drugs only)
Treated with PD-1/PD-L1 or PD-L2 monoantigens or inhibitors that have been used or used in the past. (use of combination drugs only)
Autoimmune diseases requiring systemic treatment (e.g. steroids or immunosuppressants) during the first 2 years of treatment, such as autoimmune pneumonia, glomerular nephritis, vasculitis and other symptoms of autoimmune diseases; Except for wind or child asthma. (use of combination drugs only)
Have uncontrolled primary or brain metastatic tumors
Suffering from uncontrolled mental illness, infectious diseases
The lesions cannot meet the requirements of injection capacity in the tumor body
Pregnant or lactating women
Other experimental therapies or antiviral therapy are used or are being used within 4 weeks of treatment
Other clinical studies have been taken in the past 4 weeks
Allergy to herpes virus and drug ingredients
The researchers believe that there is any reason why the patient is not suitable to participate in this trial
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