Combination of SON-1010 (IL12-FHAB) and Atezolizumab in Patients With Platinum-resistant Ovarian Cancer

• ClinicalTrials.gov Identifier: NCT05756907
• Recruitment Status: Recruiting
• First Posted: March 7, 2023
• Last Update Posted: October 23, 2023
• Sponsor: Sonnet BioTherapeutics
• Collaborator: Hoffmann-La Roche
• Information provided by (Responsible Party): Sonnet BioTherapeutics

Tracking Information

• First Submitted Date: February 23, 2023
• First Posted Date: March 7, 2023
• Last Update Posted Date: October 23, 2023
• Actual Study Start Date: September 15, 2023
• Estimated Primary Completion Date: June 30, 2024 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: February 23, 2023)

• To evaluate the safety and tolerability of SON-1010 in combination with Atezolizumab [ Time Frame: Through study completion, an average of 1 year ]
  Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
• To establish the maximum tolerated dose (MTD) of SON-1010 in combination with Atezolizumab [ Time Frame: Through study completion, an average of 1 year ]
  Incidence of dose-limiting toxicities (DLTs)

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: February 23, 2023)

To assess the anti-tumor activity of SON-1010 dosed with atezolizumab in Platinum-resistant Ovarian Cancer (PROC), compared with SON-1010 alone or SOC therapy [ Time Frame: Through study completion, an average of 1 year ]

Progression-free survival (PFS)

• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Combination of SON-1010 (IL12-FHAB) and Atezolizumab in Patients With Platinum-resistant Ovarian Cancer
• Official Title: A Proof-of-Concept Study to Assess the Combination of SON-1010 (IL12-FHAB) and Atezolizumab in Patients With Platinum-resistant Ovarian Cancer
• Brief Summary: This is a Phase 1b/2a, open-label, adaptive-design outpatient study to assess the safety, tolerability, and PK/PD of SON-1010 in combination with atezolizumab administered to patients with advanced solid tumors (Part 1) and patients with Platinum-resistant Ovarian Cancer (Part 2)
• Detailed Description: SON-1010 may work best with an immune checkpoint inhibitor (ICI), particularly with tumors that are high in the 'secreted protein acidic and rich in cysteine' (SPARC), like ovarian cancer. Immunotherapy combinations can present different toxicities, so the maximum tolerated dose (MTD) of SON-1010 with a fixed dose of atezolizumab and the recommended Phase 2 dose (RP2D) will initially be established in patients with advanced solid tumors in Part 1, with the subset of patients with platinum-resistant ovarian cancer (PROC) used in the top 2 dose cohorts. This will be followed in Part 2 with an assessment in patients with PROC of the potential for improved efficacy of the combination over SON-1010 alone, vs. the standard of care (SOC).
• Study Type: Interventional
• Study Phase: Phase 1; Phase 2
• Study Design: Allocation: Randomized; Intervention Model: Sequential Assignment; Masking: None (Open Label); Primary Purpose: Treatment

Condition

• Advanced Solid Tumor
• Platinum-resistant Ovarian Cancer

Intervention

Biological: SON-1010

SON-1010 +/- Atezolizumab

Study Arms

• Experimental: Dose Level 1
  SON-1010 Dose Level 1 + Atezolizumab
  Intervention: Biological: SON-1010
• Experimental: Dose Level 2
  SON-1010 Dose Level 2 + Atezolizumab
  Intervention: Biological: SON-1010
• Experimental: Dose Level 3
  SON-1010 Dose Level 3 + Atezolizumab
  Intervention: Biological: SON-1010
• Experimental: Dose Level 4
  SON-1010 Dose Level 4 + Atezolizumab
  Intervention: Biological: SON-1010
• Experimental: Dose Level 5
  SON-1010 Dose Level 5 + Atezolizumab
  Intervention: Biological: SON-1010
• Experimental: RP2D Expansion in Patients with Platinum-resistant Ovarian Cancer
  RP2D Dose of SON-1010 + Atezolizumab
  Intervention: Biological: SON-1010
• Experimental: Randomized Arm #1 in Patients with Platinum-resistant Ovarian Cancer
  SON-1010 @ RP2D Alone
  Intervention: Biological: SON-1010
• Experimental: Randomized Arm #2 in Patients with Platinum-resistant Ovarian Cancer
  SON-1010 @ RP2D + Atezolizumab
  Intervention: Biological: SON-1010
• No Intervention: Randomized Arm #3 in Patients with Platinum-resistant Ovarian Cancer
  Standard of Care

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Recruiting
• Estimated Enrollment (submitted: March 10, 2023): 165
• Original Estimated Enrollment (submitted: February 23, 2023): 60
• Estimated Study Completion Date: May 30, 2025
• Estimated Primary Completion Date: June 30, 2024 (Final data collection date for primary outcome measure)

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).

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Contacts

Contact: Manuel DaFonseca; 1-609-451-3900; clinical@sonnetbio.com

Contact: Richard Kenney, MD

• Listed Location Countries: Australia, United States

Administrative Information

• NCT Number: NCT05756907
• Other Study ID Numbers: SB221
• Has Data Monitoring Committee: No

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: No

• Current Responsible Party: Sonnet BioTherapeutics
• Original Responsible Party: Same as current
• Current Study Sponsor: Sonnet BioTherapeutics
• Original Study Sponsor: Same as current
• Collaborators: Hoffmann-La Roche

Investigators

• Study Director: Richard T Kenney, MD; Sonnet BioTherapeutics

• PRS Account: Sonnet BioTherapeutics
• Verification Date: October 2023