Study of STRO-002, an Anti-Folate Receptor Alpha (FolRα) Antibody Drug Conjugate in Ovarian & Endometrial Cancers

  • Interventional
  • Recruiting
  • NCT03748186
Eligibility Details Visit Clinicaltrials.gov

A Phase 1 Open-Label, Safety, Pharmacokinetic and Preliminary Efficacy Study of STRO-002, an Anti-Folate Receptor Alpha (FolRα) Antibody-Drug Conjugate (ADC), in Patients With Advanced Epithelial Ovarian Cancer (Including Fallopian Tube or Primary Peritoneal Cancers) and Endometrial Cancers

Phase 1 trial to study the safety, pharmacokinetics and preliminary efficacy of STRO-002 given intravenously every 3 weeks.

This study is a phase 1, open-label, multicenter, dose-escalation study with dose expansion to identify the maximum tolerated dose (MTD), the recommended phase 2 dose (RP2D) and to evaluate the safety, tolerability, and preliminary antitumor activity of STRO-002 in adult subjects with advanced epithelial ovarian cancer (including fallopian or primary peritoneal cancer) and endometrial cancer. Fallopian tube and primary peritoneal cancers are treated in the same manner as epithelial ovarian cancers and are thus included in this phase 1 study. Subjects eligible for this study exhibit advanced relapsed and/or progressive disease. The study will consist of 2 parts: Part 1, dose escalation, and Part 2, dose expansion.

     Part 1 (dose escalation) will enroll subjects with relapsed and/or progressive ovarian, fallopian tube or primary peritoneal cancer. Part 2 (dose expansion) will enroll subjects with relapsed and/or progressive ovarian, fallopian tube or primary peritoneal cancer (Cohort A) and subjects with relapsed and/or progressive epithelial endometrial cancer with sufficient FolRα expression per IHC as assessed by Sponsor (Cohort B).

     During dose escalation (Part 1), the initial 2 dose levels were evaluated with an N-of-1 approach followed by a standard 3+3 enrollment for all subsequent dose levels. Subjects with endometrial cancer were not enrolled in the dose escalation part of the study. Subjects were dosed based on adjusted ideal body weight (AIBW). The starting dose of 0.5 mg/kg was determined to be the human equivalent dose (HED) of 1/6 the highest non-severely toxic dose (HNSTD) identified in the good laboratory practice (GLP) toxicology study in cynomolgus monkeys. Subsequent doses follow a modified Fibonacci sequence for dose escalation, the second dose increased by 100% of the initial dose, and thereafter by 80%, 60%, 50%, 40%, 30% and then 20% of the preceding doses. The first 2 dose levels (0.5 mg/kg and 1.0 mg/kg) enrolled only 1 subject, as there was no instance of a treatment-related, clinically relevant grade 2 nonhematologic toxicity or a grade 3 hematologic toxicity of any type observed during cycle 1 (first 21 days).

     The dose escalation phase of the study was completed with the enrollment of 39 subjects over 9 dose levels (0.5-6.4 mg/kg). An MTD was not found during dose escalation. After the subjects treated at the 6.0 mg/kg dose level were reviewed by the Safety Evaluation Team, additional subjects were treated at 5.2 mg/kg, 5.6 mg/kg and 6.0 mg/kg to further characterize the safety profile. Two dose-limiting toxicity (DLT) events were observed, peripheral neuropathy at 6.0 mg/kg and bone pain at 6.4 mg/kg. Two doses, 4.3 mg/kg and 5.2 mg/kg, will be further evaluated in the dose expansion phase for safety and efficacy based on initial findings during dose escalation

     During dose expansion (Part 2), the study will enroll 2 populations, ovarian cancer (Cohort A) and endometrial cancer (Cohort B). Enrollment into Cohort A will be initiated with this protocol amendment. Subjects enrolled with ovarian cancer (including fallopian tube and primary peritoneal, Cohort A) are not required to have a minimum amount of FolRα expression, as their tumors will be assessed retrospectively by the ICH FolRα assay.

     Enrollment into Cohort B dose expansion (endometrial cancer) will not be initiated until a subsequent protocol amendment, which will define the dosing regimen and minimum FolRα expression required for study eligibility. The dose regimen for Expansion Cohort B will be selected based on Part 1 dose escalation and emerging Expansion Cohort A data (safety and pharmacokinetics [PK]). Selection of a FolRα expression cutoff for Expansion Cohort B eligibility will be determined as part of validation work with an IHC FolRα assay.

     In dose expansion, Cohort A (both dose levels) and Cohort B will be analyzed independently for preliminary efficacy.

     In both Part 1 and Part 2 of the study, STRO-002 will be dosed as an intravenous (IV) infusion on day 1 of 21-day cycles. Clinical evaluations and/or laboratory tests will be performed weekly for cycles 1-4, and at the beginning of every cycle starting with cycle 5 as described in the schedule of assessments. Samples for PK analysis will occur at specific times on days 1, 8, and 15 of cycles 1 and 4,Day 1 of cycles 2, 3, and 5 and at the end of treatment (EOT) visit. Additional clinical evaluations and lab testing may occur at the discretion of the investigator.

     Subjects who receive any dose of STRO-002 will be included in safety analyses. Disease evaluations will include peripheral blood analysis and scans as appropriate. Disease status will be evaluated per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria. Samples will be collected to assess the PK and immunogenicity of STRO-002. Biomarkers may be assessed from peripheral blood and/or tissue samples. Subjects will continue to receive study drug until disease progression, unacceptable toxicity, withdrawal of consent, or end of study (study completion).

Gender
Female

Age Group
18 Years and up

Accepting Healthy Volunteers?
No

Inclusion Criteria:

         1. Confirmation of diagnosis

         2. Evidence of measureable disease as defined by RECIST 1.1

         3. Age ≥ 18 years

         4. ECOG performance status (0-1)

         5. Life expectancy > 3 months

         6. Toxicities related to prior therapy, such as peripheral neuropathy and arthralgias must return to gr. 1 or less, except for alopecia, which can be gr. 2 or less at time of enrollment

         7. Adequate bone marrow, liver and renal functions

         8. QTcF <500 msec

         9. Ability to comply with treatment, PK and test schedules

         10. Negative pregnancy test within 7 days and use a method of birth control

         11. Relapsed and/or progressive disease: progressed after treatment with at least 2 platinum containing regimens or refractory to treatment with platinum containing therapy and with no other approved treatment options

         12. Pathological confirmation of disease under study (historical information, diagnosis, pathology report, etc)

             a. Cohort A: High-grade serous EOC, fallopian tube cancer or primary peritoneal cancer

         13. Relapsed and/or progressive disease

             Cohort A (EOC):

             - Platinum resistant and received 1-3 prior regimens or

             - Progressed after 2 prior lines of platinum therapy (regardless of platinum status) and received 2-3 prior regimens

         14. Fresh or archival tumor tissue samples must be provided to Sponsor for FolRα expression analysis as part of eligibility criteria for study entry and prior to study treatment

             1. FFPE blocks (preferably) or 10 unstained slides from the same block are required for study entry

             2. Cohort A (EOC): FolRα expression is not required for eligibility and will be assessed retrospectively post enrollment

        Exclusion Criteria:

         1. Low grade ovarian carcinoma (Grade 1).

         2. Clear cell, mucinous and sarcomatous ovarian carcinomas.

         3. Prior treatment with a FolRα-targeting ADCs or FolRα-targeting vaccines

         4. Subjects who are platinum-refractory (no response or disease progression within 3 months of completion of therapy) during frontline treatment are excluded (Expansion Cohort A [ovarian cancer] only) History of severe allergic or anaphylactic reactions to monoclonal antibody therapy or to antibody-related fusion protein treatment

         5. Greater than 3 lines of prior treatment (Expansion Cohort A [ovarian cancer] only)

         6. History of severe allergic or anaphylactic reactions to monoclonal antibody therapy or to antibody-related fusion protein treatment

         7. Prior anticancer therapy (prior to first dose of study drug): chemotherapy within 3 weeks, PARP inhibitor within 2 weeks, other therapeutic anticancer antibodies within 3 weeks, radio- or toxin-immunoconjugates (eg. ADCs) within 10 weeks, or radiation therapy/ major surgery within 2 weeks

         8. Preexisting clinically significant ocular disorders including, but not limited to: active or chronic corneal disorders, cataracts (except minor cataracts without significant visual impairment which are allowed),, glaucoma, keratitis, retinopathy, uveitis and Sjogrens syndrome. Myopia, "floaters", watering eyes are not exclusion criteria

         9. Previous solid organ transplantation

         10. Sensory or motor neuropathy ≥ grade 2

         11. Potentially fatal concurrent or recent malignancy. Subjects with past or current malignancy need to be discussed with the sponsor to determine eligibility. Examples of non-exclusionary malignancies include: cervical carcinoma Stage 1B or less; noninvasive basal cell and squamous cell skin carcinoma; localized malignant melanoma with a complete response of a duration of >10 years; low-risk in situ breast cancer treated with curative intent; superficial noninvasive bladder cancer treated with curative intent

         12. Chronic or ongoing active infectious disease requiring systemic treatment such as, but not limited to, chronic renal infection, chronic chest infection with bronchiectasis, tuberculosis and active hepatitis C

         13. Ongoing immunosuppressive therapy, including systemic corticosteroids. Note:

             Physiologic replacement and use of topical or inhaled corticosteroids are allowed.

         14. Clinically significant cardiac disease

         15. Clinically significant pre-exisiting ocular disorders

         16. Significant concurrent, uncontrolled medical condition

         17. History or clinical signs of meningeal or active CNS involvement

         18. Known severe chronic obstructive pulmonary disease or asthma

         19. History of significant cerebrovascular disease

         20. Known Human Immunodeficiency Virus seropositivity

         21. Females who are pregnant or breastfeeding, and all women of child bearing potential unwilling to use adequate barrier contraception while on treatment and for 16 weeks after last dose

         22. Positive serology for hepatitis B defined by a positive test for HBsAg

         23. Concurrent participation in another therapeutic treatment trial

At a Glance

National Government IDNCT03748186

IRB#IRB18-1573

Lead SponsorSutro Biopharma, Inc.

Lead PhysicianJohn Moroney

Collaborator(s)N/A

EligibilityFemale
18 Years and up
Recruiting