Combining SON-1010 and Atezolizumab for treating platinum-resistant ovarian cancer

A Proof-of-Concept Study to Assess the Combination of SON-1010 (IL12-FHAB) and Atezolizumab in Patients With Platinum-resistant Ovarian Cancer

This study is testing a new immune therapy called SON-1010 combined with atezolizumab to see if it helps people with advanced platinum-resistant ovarian cancer feel better compared to standard treatments.

Quick facts

• Phase: Phase1; Phase2
• Study type: Interventional
• Enrollment: 165 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: Sonnet BioTherapeutics (Industry-sponsored)
• Drugs / interventions: immunotherapy, prednisone, atezolizumab
• Locations: 4 sites (Santa Monica, California and 3 other locations)
• Trial ID: NCT05756907 on ClinicalTrials.gov

What this trial studies

This clinical trial evaluates the safety and effectiveness of SON-1010, an immune therapy, in combination with atezolizumab for patients with advanced solid tumors, specifically focusing on those with platinum-resistant ovarian cancer. The study is divided into two parts: the first part establishes the maximum tolerated dose of SON-1010 alongside a fixed dose of atezolizumab, while the second part assesses the efficacy of this combination compared to standard care. The trial is designed to adapt based on findings from the initial phase, allowing for a tailored approach to treatment.

Who should consider this trial

Good fit: Ideal candidates include adults aged 18 and older with histologically confirmed platinum-resistant ovarian cancer who have exhausted standard treatment options.

Not a fit: Patients with early-stage ovarian cancer or those who have not yet received standard treatment may not benefit from this study.

Why it matters

Potential benefit: If successful, this combination therapy could provide a new treatment option for patients with platinum-resistant ovarian cancer, potentially improving outcomes.

How similar studies have performed: Other studies have shown promise with similar immunotherapy combinations, indicating potential for success in this approach.

Eligibility criteria

Inclusion Criteria:

1. Age ≥18 years at the time of informed consent
2. Part 1: Must have histologically or cytologically verified solid tumors and patients must have locally advanced or metastatic disease. Must have been treated with standard of care therapies for their disease and have no standard alternative treatment options that are deemed by the treating physician to offer reasonable or potentially better benefit. Patients in cohorts C4, C5, and the RP2D expansion group must have PROC.

   Part 2: Must have PROC, defined as recurrence of OC within 6-months (180-days) after the last dose of a platinum-containing regimen), including epithelial, fallopian tube, or 1° peritoneal carcinoma. Patients may have had one or more alternative regimen(s) before this trial, including maintenance therapy between consecutive lines of therapy. Evidence of progression and the timing of progression or reoccurrence must refer to new measurable disease by RECIST v1.1 or evaluable (non-measurable) disease. The latter is defined as not having measurable disease but has pre-study baseline values of CA125 at least 2 x ULN, with ascites and/or pleural effusion attributed to tumor OR with solid and/or cystic abnormalities on radiographic imaging consistent with recurrent disease that do not meet RECIST 1.1 definitions for target lesions.
3. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1.
4. Adequate organ and bone marrow function, in the absence of growth factors.
5. Females of childbearing potential, or \< 1-year postmenopause who are not permanently sterile, must have a negative serum pregnancy test (beta-human chorionic gonadotropin \[β-HCG\]) at baseline, and agree to use 2 highly effective methods of birth control during the study and for 30 days after the last dose of study drug. Females who are not of childbearing potential (have had a tubal ligation, hysterectomy, or bilateral oophorectomy, or are ≥ 1-year postmenopause) or have a partner who has had a vasectomy do not need to use contraception. A follicle stimulating hormone (FSH) level \> 35 IU/L at screening will be performed to confirm status. Refer to Section 8.2.7 for further detail.
6. Males and their female partners must use a highly effective method of birth control if female partner(s) is of childbearing potential and must not donate sperm during the study and for 90 days after the last dose of study drug.
7. Willing and able to provide signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

Exclusion Criteria:

1. Known history of allergy to any component of study drug or a history of severe allergic/anaphylactic reaction.
2. Hospitalization for subacute bowel obstruction, other complications of the cancer, or any major surgery within 28 days prior to C1D1. Elective surgery is allowed if recovered.
3. Infection with HIV-1 or HIV-2 or a history of Kaposi sarcoma and/or Multicentric Castleman Disease.
4. Current active liver disease from any cause, including hepatitis A (hepatitis A virus IgM positive), hepatitis B (hepatitis B virus \[HBV\] surface antigen positive), or hepatitis C (hepatitis C virus \[HCV\] antibody positive, confirmed by HCV ribonucleic acid). Patients with HCV with undetectable virus after treatment are eligible (note: patients must have completed curative anti-viral therapy at least 4 weeks prior to screening). Patients with a prior history of HBV are eligible if quantitative PCR for HBV DNA is negative (note: patients must have received HBV antiviral therapy for at least 4 weeks prior to screening)
5. Pregnancy and/or lactation
6. Has received a live or live-attenuated vaccine within 30 days prior to the first dose of study drug. (Note: Administration of killed vaccines and COVID-19 vaccines that are not live or live-attenuated are allowed if \> 14 days.)
7. History of any active infection requiring systemic antibiotics, antivirals or antifungals, including COVID-19, within 14 days before the first dose of study drug.
8. Any acute noninfectious illness not resolved by14 days before day 1.
9. History of or known or suspected autoimmune disease (exception(s): patients with vitiligo, Type I diabetes, resolved childhood atopic dermatitis, hypothyroidism, or hyperthyroidism that is clinically euthyroid at Screening are allowed). Other exceptions may be allowed following discussion with the Sponsor Medical Monitor for patients who have not received treatment for their autoimmune disorder in the past 3 years
10. Known active central nervous system metastases and/or carcinomatous meningitis. Patients with previously treated brain metastases may participate provided they are clinically stable for at least 4 weeks prior to study entry and have no evidence of new or enlarging brain metastases.
11. Unresolved toxicities from prior anticancer therapy, defined as not resolved to baseline or to Grade 1 (NCI 2017), except for alopecia, peripheral neuropathy, and hypothyroidism secondary to prior therapy if currently being treated and clinically euthyroid.
12. Receipt of any investigational agent or treatment within 21 days or 5 half-lives, whichever is shorter, before the first dose of study drug.
13. Any prior immunotherapy or treatment with checkpoint inhibitors within a period of 5 half-lives (or 3 months, whichever is shorter) since the last dose of the therapy.
14. Use of systemic steroids \> 10 mg/day prednisone (or equivalent) within 10 days of enrollment, except for local (topical, nasal, or inhaled) steroid use. Limited doses of systemic steroids (e.g., in patients with exacerbation of reactive airway disease) must have completed at least 10 days before enrollment. Steroid use to prevent IV contrast allergic reaction or anaphylaxis in patients who have known contrast allergies is allowed at any time before enrollment.
15. Active known second malignancy with the exception of any of the following:

    * Adequately treated basal cell carcinoma, squamous cell carcinoma of the skin, or in situ cervical cancer
    * Adequately treated Stage I cancer from which the patient is currently in remission and has been in remission for ≥ 2 years;
    * Low-risk prostate cancer with Gleason score \< 7 and prostate-specific antigen \< 10 ng/mL; or
    * Any other cancer from which the patient has been disease-free for ≥ 2 years.
16. Use of biotin (i.e., vitamin B7) or supplements containing biotin higher than the daily adequate intake of 30 μg (FDA 2019) (Note: Patients who switch from a high dose to a dose of 30 μg/day or less are eligible for study entry)
17. Any of the following within 6 months before Baseline Day 1:

    * Myocardial infarction;
    * Unstable angina;
    * Unstable symptomatic ischemic heart disease;
    * New York Heart Association (NYHA) class III or IV heart failure;
    * Thromboembolic events (e.g., deep vein thrombosis, pulmonary embolism, or symptomatic cerebrovascular events);
    * Any other significant cardiac condition (e.g., pericardial effusion, restrictive cardiomyopathy, severe untreated valvular stenosis, long QTc syndrome, or severe congenital heart disease).

Where this trial is running

Santa Monica, California and 3 other locations

• Sarcoma Oncology Center — Santa Monica, California, United States (Recruiting)
• The Border Cancer Hospital — Albury, New South Wales, Australia (Recruiting)
• Blacktown Mt Druitt Hospital — Blacktown, New South Wales, Australia (Recruiting)
• Ashford Cancer Centre Research — Kurralta Park, South Australia, Australia (Recruiting)

Study contacts

• Study coordinator: Manuel DaFonseca

Conditions Advanced Solid Tumor; Platinum-resistant Ovarian Cancer