Trial Search Results

A Phase Ib Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Cibisatamab in Combination With Atezolizumab After Pretreatment With Obinutuzumab in Participants With Previously Treated Metastatic Colorectal Adenocarcinoma

CO40939 is a Phase Ib, open-label, multicenter, single-arm study designed to evaluate the safety, efficacy, pharmacokinetics, and immunogenicity of cibisatamab in combination with atezolizumab administered after pretreatment with obinutuzumab in patients with Stage IV microsatellite stable (MSS) metastatic colorectal cancer (mCRC) whose tumors have high carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) expression and who have progressed on two or more chemotherapy regimens. The study is composed of a safety run-in and an exploratory part.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Hoffmann-La Roche

Stanford Investigator(s):

Intervention(s):

  • Drug: Obinutuzumab
  • Drug: Atezolizumab
  • Drug: Cibisatamab
  • Drug: Tocilizumab

Phase:

Phase 1

Eligibility


Inclusion criteria

   - Histologically confirmed adenocarcinoma originating from the colon or rectum

   - Metastatic disease not amenable to local treatment

   - Tumors that are microsatellite stable or microsatellite instability low, as determined
   by a local, certified laboratory

   - Tumors that have high carcinoembryonic antigen-related cell adhesion molecule 5
   (CEACAM5) expression as determined by quantitative reverse transcription polymerase
   chain reaction (qRT-PCR) in an archival tumor sample or a fresh tumor biopsy and
   documented through central testing of a representative tumor tissue specimen performed
   at baseline

   - Experienced disease progression during or within 3 months following the last
   administration of approved standard therapies

   - Eastern Cooperative Oncology Group Performance Status of 0 or 1

   - Life expectancy of >= 12 weeks

   - Adequate hematologic and end-organ function

   - Negative HIV test at screening

   - Negative hepatitis B surface antigen test and total hepatitis B core antibody (HBcAb)
   test at screening, or positive total HBcAb test followed by a negative hepatitis B
   virus (HBV) DNA test at screening

   - Negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody
   test followed by a negative HCV RNA test at screening

   - Negative human T-cell lymphotropic virus type 1 test for participants from endemic
   countries (Japan, countries in the Caribbean basin, South America, Central America,
   sub-Saharan Africa, and Malaysia)

   - For women of childbearing potential: agreement to remain abstinent or use
   contraceptive methods, agreement to regular pregnancy testing, and agreement to
   refrain from donating eggs, women must remain abstinent or use contraceptive methods
   with a failure rate of < 1% per year during the treatment period and for 5 months
   after the final dose of atezolizumab, for 4 months after the final dose of
   cibisatamab, for 18 months after the final dose of obinutuzumab, and for 3 months
   after the final dose of tocilizumab

   - For men: agreement to remain abstinent or use a condom, and agreement to refrain from
   donating sperm, with a female partner of childbearing potential or pregnant female
   partner, men must remain abstinent or use a condom during the treatment period and for
   3 months after the final dose of cibisatamab, for 3 months after the final dose of
   obinutuzumab, and for 2 months after the final dose of tocilizumab to avoid exposing
   the embryo

   - Lactic acid dehydrogenase (LDH)
Additional Inclusion Criteria for patient enrollment into Part 2 of the study:

- No prior treatment with regorafenib or Trifluridine/Tipiracil (TAS-102)

Exclusion criteria

   - Symptomatic, untreated, or actively progressing central nervous system metastases

   - Non-irradiated tumor lesions > 2 cm at critical sites where tumor swelling induced by
   cibisatamab is expected to lead to significant complications

   - Dyspnea or peripheral capillary oxygen saturation < 92% at rest at baseline for
   patients with bilateral lung lesions or metastases in the remaining lung following
   lobectomy or pneumonectomy

   - Spinal cord compression not definitively treated with surgery and/or radiation or
   previously diagnosed and treated spinal cord compression without evidence that disease
   has been clinically stable for >= 2 weeks prior to initiation of study treatment

   - History of leptomeningeal disease and progressive multifocal leukoencephalopathy

   - Uncontrolled tumor-related pain and pleural effusion or ascites requiring recurrent
   drainage procedures

   - Participants with pericardial effusion

   - Uncontrolled or symptomatic hypercalcemia

   - Active or history of autoimmune disease or immune deficiency

   - History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced
   pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening
   chest computed tomography scan

   - Active tuberculosis that has required treatment within 3 years prior initiation of
   study treatment or latent tuberculosis that has not been appropriately treated

   - Uncontrolled hypertension, unstable angina, congestive heart failure of any New York
   Heart Association Class II or greater, serious cardiac arrhythmia requiring treatment
   and history of myocardial infarction within 6 months prior to initiation of study
   treatment

   - Major surgical procedure, other than for diagnosis, within 4 weeks prior to initiation
   of study treatment, or anticipation of need for a major surgical procedure during the
   study

   - History of malignancy other than CRC within 5 years prior to screening, with the
   exception of malignancies with a negligible risk of metastasis or death, such as
   adequately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma,
   localized prostate cancer, ductal carcinoma in situ, or Stage I uterine cancer

   - Known active infection, or reactivation of a latent infection, whether bacterial,
   viral, fungal, mycobacterial, or other pathogens, or any major episode of infection
   requiring hospitalization or treatment with IV antibiotics

   - Prior allogeneic stem cell or solid organ transplantation

   - Any other disease, metabolic dysfunction, physical examination finding, or clinical
   laboratory finding that contraindicates the use of an investigational drug, may affect
   the interpretation of the results, or may render the patient at high risk from
   treatment complications

   - Treatment with a live, attenuated vaccine within 4 weeks prior to initiation of study
   treatment, or anticipation of need for such a vaccine during study treatment or within
   5 months after the final dose of atezolizumab

   - Current treatment with anti-viral therapy for HBV

   - Treatment with any systemic anti-cancer therapy, including chemotherapy or hormonal
   therapy, within 28 days prior to initiation of study treatment

   - Treatment with investigational therapy within 28 days prior to initiation of study
   treatment

   - Prior treatment with any of the protocol-specified study treatments

   - Prior treatment with T-cell bispecifics (TCBs), including CEACAM5-TCB, CD137 agonists
   or immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, and
   anti-PD-L1 therapeutic antibodies

   - Treatment with systemic immunostimulatory agents within 4 weeks or 5 half-lives of the
   drug prior to initiation of study treatment

   - Treatment with systemic immunosuppressive medication within 2 weeks prior to
   initiation of study treatment, or anticipation of need for systemic immunosuppressive
   medication during study treatment

   - Adverse events from prior anti-cancer therapy that have not resolved to Grade 1 or
   better with the exception of alopecia of any grade and Grade <= 2 peripheral
   neuropathy

   - History of severe allergic anaphylactic reactions to chimeric or humanized antibodies
   or fusion proteins

   - Known hypersensitivity to Chinese hamster ovary cell products

   - Known allergy or hypersensitivity to any of the study drugs or any of their excipients

   - Pregnancy or breastfeeding, or intention of becoming pregnant during study treatment
   or within 5 months after the final dose of atezolizumab, within 4 months after the
   final dose of cibisatamab, within 18 months after the final dose of obinutuzumab, and
   within 3 months after the final dose of tocilizumab

   - Participants with pleural effusion requiring drainage procedures

   - Participants with pleural effusion and/or pleural lesions involving both lungs (i.e.
   bilateral pleural effusions; unliateral pleural effusion with pleural lesion in the
   contralateral lung)

   - Participants with >10 bilateral pulmonary lesions (i.e. at least one lesion in each
   lung and more than 10 lung lesions in total)

   - Participants with pulmonary miliary metastatic pattern (innumerable small lesions) or
   pulmonary lymphangitic carcinomatosis

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Smruti Rahalkar
650-498-5186
Not Recruiting