About this trial
Oncolytic virus product named Olvi-Vec combined with Platinum plus Etoposide in patients with late phase SCLC
Eligibility criteria
Qualifiers
Able to understand and voluntarily sign an informed consent form.
Age ≥ 18 years old, gender not limited.
Small cell lung cancer confirmed by organization or cytology.
After receiving platinum based chemotherapy regimens and/or immunotherapy, platinum based chemotherapy regimens and/or anlotinib, and other recommended treatments according to guidelines, disease progression or recurrence has occurred.
Disqualifiers
Compound small cell lung cancer and transformed small cell lung cancer.
Patients with brain metastases and neurological symptoms; Note: Subjects with previous imaging evidence of brain metastases who have undergone local treatment (such as radiotherapy or surgery) for intracranial metastases and have stable lesions for more than 28 days without symptoms can be enrolled.
Other primary malignant tumors other than small cell lung cancer (excluding non melanoma skin cancer, breast cancer in situ, cervical cancer in situ, and superficial bladder cancer, or other cancers that have been effectively controlled in the past three years and have no evidence of disease recurrence) were previously or currently combined.
Clinically significant cardiovascular diseases At the beginning of the study treatment, the toxicity associated with previous anti-tumor treatments did not recover to ≤ CTCAE grade 1, except for hair loss and peripheral neurotoxicity of CTCAE grade 2.
Trial design
Treatments tested in this trial
- Olvi-Vec
- platinum (cisplatin or carboplatin)
- Etoposide
Treatment groups
Sponsors and collaborators
Newsoara HYK Biopharmaceutical (Shanghai) Co., Ltd.
Lead sponsor
Genelux Corporation
Collaborator