SI-B036: SI-B036 will be administered on Day 1 by intravenous (IV) infusion every 3 weeks
Study summary
The objective of the study is to evaluate the safety and tolerability of SI-B036 in participants with solid tumors who have received at least one prior line of therapy for advanced disease.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Documented locally advanced or metastatic solid tumor(s) not amenable to curative surgery or radiation and have received at least 1 line of standard therapy, including adjuvant/neoadjuvant treatment, or whose cancer is considered refractory to the standard of care (SOC) or for which no standard treatment is available.
* Toxicity of previous antitumor therapy has returned to level ≤1 as defined by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) V6.0.
* Has no serious cardiac dysfunction and left ventricular ejection fraction ≥50%.
* Has adequate organ function before enrollment
PART C Additional Inclusion Criteria (Dose Expansion Only)
\- For immuno-oncology (IO)-exposed non-small cell lung cancer (NSCLC): histologically or cytologically confirmed unresectable locally advanced or metastatic non-small cell lung cancer (NSCLC) in subjects who are previously exposed to immune checkpoint inhibitor (ICI) therapy (IO-exposed) and whose disease is refractory to standard of care (SOC) therapy or for whom no appropriate standard treatment options are available. In addition, subjects must have received at least one prior line of platinum therapy.
For IO naïve NSCLC: histologically or cytologically confirmed unresectable locally advanced or metastatic NSCLC in subjects who are not previously exposed to ICI therapy. Subjects must also have PD-L1 expression ≥1% (tumor proportion score \[TPS\]) as determined by an FDA-approved assay. In addition, subjects must have received at least one prior line of platinum therapy.
For Melanoma: histologically confirmed unresectable or metastatic melanoma with prior treatment with an immune checkpoint inhibitor regimen and documented disease progression following such therapy.
For Ovarian Cancer: has histologic documentation of epithelial ovarian, primary peritoneal, or fallopian tube cancer that has progressed or relapsed on or after a previous chemotherapy with or without a poly (ADP-ribose) polymerase (PARP) inhibitor. Prior bevacizumab treatment is allowed.
Exclusion Criteria:
* Chemotherapy, biological therapy, immunotherapy, targeted therapy (including small molecule inhibitor of tyrosine kinase), and other antitumor therapy within 4 weeks or 5 half-lives (whichever is shorter) prior to the first administration; radical radiotherapy, major surgery within 4 weeks prior to the first administration; mitomycin and nitrosoureas treatment within 6 weeks prior to the first administration; oral drugs such as Ticio such as capecitabine, or palliative radiotherapy within 2 weeks prior to initial administration.
* Received systemic immunostimulatory therapy within 4 weeks prior to the first dose or is still within 5 half-lives of the treatment (whichever is longer).
* Received immunosuppressive drugs within 2 weeks prior to the first dose. The use of topical, inhaled, and locally injected steroids is permitted.
* Participants with history of severe heart disease within 6 months before enrollment.
* Participants with prolonged QT interval (QTcF \>470 msec), complete left bundle branch block, Grade 3 atrioventricular block, or a history of additional risk factors for Torsades de Pointes (TdP) or any current concomitant medication known to prolong the QT/QTc interval or cause TdP.
* Other malignant tumors were diagnosed within 5 years prior to the first administration.
* For the dose escalation portion of the study only, participants with a primary diagnosis of lung cancer are excluded.
* Participants with a thromboembolic event (eg, deep vein thrombosis \[DVT\] or pulmonary embolism \[PE\]), stroke, or transient ischemic attack (TIA) within 6 months before screening.
* Participants with active or recent clinically significant bleeding are excluded, or who are at risk of bleeding due to clinically significant platelet abnormalities or coagulopathy, or who require full-dose anticoagulation or high-intensity antiplatelet therapy on high dose nonsteroidal anti-inflammatory drugs (NSAIDs).
* Active autoimmune diseases and inflammatory diseases. For autoimmune conditions that are active but stable and low-grade on systemic therapy, discussion with the medical monitor is required prior to screening.
* Participants with advanced/clinically significant lung diseases, who have a history of noninfectious interstitial lung disease (ILD)/pneumonitis that required treatment with steroids, have current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening, or concurrent pulmonary disease resulting in severe impaired respiratory function.
* Participants with primary tumors in the central nervous system (CNS), active or untreated CNS metastases or carcinomatous meningitis should be excluded. Participants with previously treated brain metastases may participate provided they are clinically stable for at least 4 weeks and have no evidence of new or enlarging brain metastases and no requirements for corticosteroids 14 days prior to Screening.
* Participant with active or untreated hemorrhagic CNS lesions.
* Participants with a history of anaphylaxis or severe hypersensitivity reactions.
* Previous organ transplantation or allogeneic hematopoietic stem cell transplantation.
* Subjects with recent surgery, biopsy, or invasive procedures without adequate wound healing prior to study enrollment.
* Participated in another clinical trial within 4 weeks prior to first dose of study treatment.
* Participants who are pregnant, breastfeeding, or planning to become pregnant during the study.
* History of fistula, gastrointestinal perforation, or abdominal abscess within 6 months prior to the first dose.
* Participant with moderate or major hemoptysis history.
* Participant has tumors invading large blood vessels
* Other conditions that the Investigator or sponsor believes are not suitable for participating in this clinical trial.
Primary outcome measure(s)
Participants with Dose-Limiting Toxicities — 24 months A DLT is defined as any of the following:
* Grade 4 neutrophil count decreased lasting \>7 days.
* Grade ≥3 febrile neutropenia of any duration.
* Grade ≥3 platelet count decreased with clinically significant hemorrhage.
* Grade 4 thrombocytopenia lasting \>72 hours
* Death not related to disease progression or extraneous cause.
* Hy's law cases
* Grade ≥3 infusion-related reactions (IRRs) leading to permanent discontinuation
* Grade ≥3 non-hematologic toxicities, except for:
* Grade 3 nausea/vomiting or diarrhea for \<72 hours with adequate antiemetic and other supportive care;
* Grade 3 fatigue for less than 1 week;
* Grade ≥3 electrolyte abnormality that lasts up to 72 hours, is not clinically complicated, and resolves spontaneously or responds to conventional medical interventions;
* Grade ≥3 amylase or lipase that is not associated with symptoms or clinical manifestations of pancreatitis and does not require hospitalization
Participants with Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESIs), and Treatment-Emergent Adverse Events (TEAEs) — 24 months Measuring the number of patients with serious adverse events (SAEs), Adverse Events of Special Interest (AESIs), and Treatment-Emergent Adverse Events (TEAEs)
Participants with abnormal physical examination findings — 24 months Measure the number of participants with abnormal physical examination findings.
Participants with abnormal lab results — 24 months Measure the number of participants with abnormal clinical laboratory values
Participants with abnormal ECG reading — 24 months Patients with abnormal ECG parameters (including the change from-baseline ECG parameters: heart rate \[HR\]; PR; QTcF; and QRS intervals \[∆HR, ∆PR, ∆QTcF, and ∆QRS\])
To determine the maximum tolerated dose (MTD) if reached or minimum safe and pharmacologically effective dose (MSED). — 24 months The actual number of subjects enrolled and dose levels to be explored in this study will depend on the MTD and/or MSED based on DLTs reported during the DLT observation period.
Trial sites (7)
Facility
City
Region
Status
Yale Cancer Center
New Haven
Connecticut
Florida Cancer Specialists Lake Nona
Orlando
Florida
Florida Cancer Specialists Sarasota
Sarasota
Florida
OU Health Stephenson Cancer Center
Oklahoma City
Oklahoma
Sarah Cannon Research Institute - Oncology Partners
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
We use cookies to analyse site traffic and improve your experience. With your consent, we may also use cookies for advertising. You can change your choice at any time.