Study of SMT-NK Inj. Plus Pembrolizumab vs Pembrolizumab Monotherapy in Patients With Advanced Biliary Tract Cancer

Randomized, Placebo-controlled, Open-label, Phase 2b Clinical Trial to Evaluate the Antitumor Activity of Combination Therapy of SMT-NK and Pembrolizumab vs Pembrolizumab Monotherapy in Patients With Advanced Biliary Tract Cancer

This study is designed to assess the antitumor activity of combination therapy of SMT-NK (allogeneic natural killer cells) and pembrolizumab versus pembrolizumab monotherapy in patients with advanced biliary tract cancer

Study Overview

• Status: Recruiting
• Conditions: Biliary Tract Cancer
• Intervention / Treatment: Drug: Pembrolizumab; Drug: SMT-NK inj.+Pembrolizumab

Detailed Description

The term of biliary tract cancer (BTC) refers to all tumors that arise from the biliary tract or the biliary drainage system, including the gallbladder.Biliary tract cancer is one of the most poorly prognosis cancers and the five-year survival rate remains at about 10% as it is difficult to expect long-term survival due to frequent local recurrence and remote metastasis after surgery.

South Korea belongs to a country with a high number of biliary tract cancer patients, and the incidence of biliary tract cancer is actually increasing every year.According to the 2018 National Cancer Registration Statistics, the number of 5-year biliary tract cancer patients was 13,967 (7,547 men and 6,420 women), which corresponds to about 2.9% of all cancersand the 5-year survival rate of biliary tract cancer patients between 2014 and 2018 was 28.8%, showing a lower survival rate than other cancer species.

Most of the long-term survival is due to early detection by screening, but advanced carcinoma is a refractory carcinoma with a 5-year survival rate of less than 5%.In addition to standard anticancer drugs, alternative anticancer drugs and targeted treatments can be developed for cancer with a large number of patients, but biliary tract cancer is difficult to find any more treatments if standard treatment fails and standard anticancer treatments cannot be continued due to resistance.

Natural killer cells (NK cells) are innate lymphocyte cells with cell killing activity, and have the characteristic of destroying cells by secretion of and granzyme into cancer cells and abnormal cells that are reduced or deficient in expression of MHC class I.Clinical studies using natural killer cells as anticancer drugs have long been conducted on various cancers.

Pembrolizumab is a monoclonal antibody designed to bind to a receptor called PD-1, which is expressed by immune cells such as T cells.Natural killer cells were also found to be expressing PD-1 in the same way as T cells, and in particular, PD-1 was found to be higher in cancer patients than in healthy people.

Therefore, combined therapy with the immune-check point such as pembrolizumab can be useful in elevating the anticancer activity of NK cells.

• Study Type: Interventional
• Enrollment (Anticipated): 128
• Phase: Phase 2; Phase 3

Contacts and Locations

• Study Contact: Name: JUNGMIN IM; Phone Number: 82-02-6297-0515; Email: jungminim@smtbio.co.kr
• Study Contact Backup: Name: HAEJIN IM; Phone Number: 82-02-6297-0515; Email: imjin@smtbio.co.kr

Study Locations

• Korea, Republic of
  • Seoul, Korea, Republic of, 06273
    • Recruiting
    • Gangnam Severance Hospital
    • Contact: Sung Ill Jang, MD. PhD; Phone Number: 82-2-2019-3580; Email: AEROJSI@yuhs.ac
  • Seoul, Korea, Republic of, 03722
    • Recruiting
    • Severance Hospital
    • Contact: Seung Woo Park, MD. PhD; Phone Number: 82-2-2228-1964; Email: SWOOPARK@yuhs.ac
  • Gyeonggi-do
    • Goyang-si, Gyeonggi-do, Korea, Republic of, 10408
      • Recruiting
      • National Cancer Center
      • Contact: SANGMYUNG WOO; Phone Number: 82-31-920-1733; Email: wsm@ncc.re.kr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 19 years to 80 years (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Patients who received a histopathological or cytologic diagnosis of nonresectable, advanced biliary tract carcinoma (intrahepatic or extrahepatic cholangiocarcinoma, gallbladder cancer) and patients with refractory disease after chemotherapy and/or patients who have difficulty with chemotherapy due to side effects of chemotherapy.
2. Patients who receives an explanation from the trial manager about the purpose, contents, and characteristics of the Investigational products for the clinical trial and is signed by the person, guardian or legal representative in the written informed consent.
3. 19 to 80 years old on day of signing informed consent.

4. Histopathological or cytologic diagnosis of advanced adenocarcinoma of the biliary tract and those with measurable lesions for RECIST evaluation

   • Tumor lesion: Must be accurately measured in at least one dimension (longest diameter in the plane of measurement is to be recorded) with a minimum size of 10mm by CT scan
   • Malignant lymph nodes: To be considered pathologically enlarged and measurable, a lymph node must be ≥15mm in short axis when assessed by CT scan
5. Have a performance status of ≤2 on the ECOG Performance Scale.
6. Patients who survival period is expected to be at least 3 months.

7. Demonstrate laboratory test results the following conditions:

   • ANC (Absolute Neutrophil Count) ≥ 1,500/μL
   • Hemoglobin≥ 9 g/dL
   • Platelet> 80,000/μL
   • serum BUN & Creatinine ≤ 2.0 x upper limit of normal (ULN)
   • AST & ALT ≤ 5.0 x upper limit of normal (ULN)
   • Bilirubin ≤ 5mg/dL
   • Albumin ≥ 2.8g/dL
   • Prothrombin time (PT)% activity ≥ 70%
8. Patients or partners who has agreed to the appropriate use of contraceptives by two or more during the treatment period (including Survival follow-up period) (for men, those who have agreed not to provide sperm)

9. Patients who meet one or more of the following conditions:

   • Patients have at least 1% Combined Positive Score (*CPS) PD-L1 expression detected on the tumor, as determined by **immunohistochemistry performed by a central laboratory.

     • CPS = (number of PD-L1 positive tumor cells, lymphocytes, macrophage)/ (total number of viable tumor cells) X 100

     • Immunohistochemistry: IHC 22C3 pharmDx test

       ② Patients who have a positive MSI-H or dMMR test

       • MSI-high positive tumors analyzed by PCR
       • dMMR positive tumors analyzed by immunohistochemical staining
     • MSI-H was measured by PCR, and positive finding when two or more unstable markers were detected in PCR for 5 microsatellite markers, **dMMR is analyzed by immunohistochemical staining and positive when the discovery of one or more genes in MLH1, MSH2, MSH6 and PMS2 staining is lost.

Exclusion Criteria:

1. Patients who have previous history

   • Immune deficiency or autoimmune disease that can be aggravated by immunotherapy (for example: Rheumatoid arthritis, systemic lupus erythematosus, vasculitis, multiple sclerosis, Crohn's disease, ulcerative colitis, adolescent-developed insulin-dependent diabetes mellitus).
   • Immune deficiency disease
   • Pneumonia, colitis, hepatitis, nephritis, endocrine diseases associated with immunodeficiency (hypophysis, thyroid dysfunction, Type 1 diabetes, etc.)
   • Obvious myocardial failure or uncontrolled arterial hypertension
   • Active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   • Non-infectious pneumonia, interstitial lung disease
   • Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
   • Hepatitis B (defined as HBsAg reactive) or known active hepatitis C virus (defined as HCV ribonucleic acid (RNA) [qualitative] is detected) infection or active tuberculosis
   • Active infection (if systemic treatment is required)
2. Has a diagnosed and/or treated additional malignancy within 5 years prior to signing informed consent except for curatively treated basal cell carcinoma of the skin, squamous cell carcinoma of the skin
3. Has a previous history of anti-angiogenic agent treatment before signing informed consent
4. Has a known serious allergic history
5. Has a known serious mental illness

6. Identified the following in Screening:

   • CRP ≥10 mg/dl and albumin ≤3.0 g/dl are suspected of cancer cachexia
   • Patients who have symptomatic ascites that is not controlled by medical treatment
7. Has received chemotherapy not less than 4 weeks old before randomization
8. Has received a live vaccine within 4 weeks before randomization
9. Is currently participating in or has participated in another clinical study within 4 weeks before randomization or the adverse event due to investigational drug administered remain before randomization
10. Has previously administrated Pembrolizumab and another anti-PD-1/PD-L1 agent
11. Has previously administrated immune-cell therapy (including natural killer cell etc.)
12. Female who are pregnant, breastfeeding or intending to become pregnant during the study period.
13. Has a history of any contraindication or has a severe hypersensitivity to any components of pembrolizumab
14. Has performed major surgery within 4 weeks prior to signing informed consent
15. Patients who are unsuitable to participate in clinical trials by investigator's decision

Study Plan

How is the study designed?

Design Details

• Primary Purpose: TREATMENT
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: Pembrolizumab+SMT-NK inj.; Experimental: Pembrolizumab + SMT-NK inj. Participants will be randomized to receive 200 mg pembrolizumab followed by 3*10^6cells/kg SMT-NK inj. Interventions: Drug: SMT-NK inj. Drug: Pembrolizumab	Drug: SMT-NK inj.+Pembrolizumab; SMT-NK inj. will be administered as an intravenous (IV) infusion on Day 1,Day 7 of each 21-day cycle. Pembrolizumab will be administered as an intravenous (IV) infusion every 3 weeks on Day 1 of each 21-day cycle.
PLACEBO_COMPARATOR: Pembrolizumab; Placebo Comparator: Pembrolizumb Participants will be randomized to receive 200 mg pembrolizumab. Intervention: Drug: Pembrolizumab	Drug: Pembrolizumab; Pembrolizumab will be administered as an intravenous (IV) infusion every 3 weeks on Day 1 of each 21-day cycle.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Progression Free Survival	Progression-free survival (PFS) is defined as the time from the date of initial administration of the clinical trial drug to the progression or death due to any cause of the disease	Up to approximately 72 weeks from the date of first administration of clinical trial drugs

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Object Response rate	Objective response rate (ORR) is defined as the ratio of subjects whose best overall response (hereinafter referred to as BOR) is partial response (PR) or complete response (CR) assessed by RECIST Version 1.1 and iRECIST.	Up to approximately 72 weeks from the date of first administration of clinical trial drugs
Time to Progression	Time to disease progression (TTP) is defined as the time from the first administration date of the clinical trial drug to the first disease progression	Up to approximately 72 weeks from the date of first administration of clinical trial drugs
Overall Survival	Overall survival(OS) is defined as the time from the date of first administration of the clinical trial drug to the death of all causes	Up to approximately 120 weeks from the date of first administration of clinical trial drugs
Duration of Response	Duration of Response (DoR) is defined as the time from the date of the first documentation of objective response (confirmed CR or confirmed PR) to the date of the first disease progression or death due to any cause.	Up to approximately 72 weeks from the date of first administration of clinical trial drugs
Disease Control Rate	Disease Control Rate (DCR) is defined as the proportion of participants who achieved a BOR of confirmed CR, confirmed PR, or stable disease (SD), assessed by RECIST Version 1.1 and iRECIST	Up to approximately 72 weeks from the date of first administration of clinical trial drugs
Best Overall Response	In order for the best overall response (BOR) to be finally evaluated as partial response (PR) or complete response (CR), it must be evaluated as partial response (PR) or complete response (CR) in two consecutive evaluations by RECIST Version 1.1 and iRECIST.	Up to approximately 72 weeks from the date of first administration of clinical trial drugs
Time to Response	The time to response (TTR) is defined as the time from the date of first administration of the clinical trial drug to the time when it is evaluated as the first partial response (PR) or full response (CR) by RECIST Version 1.1 and iRECIST.	Up to approximately 72 weeks from the date of first administration of clinical trial drugs
Quality of Life	Assessed by EORTC-QLQ(The European Organization for Research and Treatment-QoL questionnaire) C30	Up to approximately 72 weeks from the date of first administration of clinical trial drugs

Collaborators and Investigators

• Sponsor: SMT bio Co., Ltd.
• Investigators: Principal Investigator: SEUNGWOO PARK, Department of Internal Medicine, Yonsei University College of Medicine, Severance Hospital

Study record dates

Study Major Dates

• Study Start (ACTUAL): June 9, 2022
• Primary Completion (ANTICIPATED): January 8, 2025
• Study Completion (ANTICIPATED): June 8, 2026

Study Registration Dates

• First Submitted: June 17, 2022
• First Submitted That Met QC Criteria: June 17, 2022
• First Posted (ACTUAL): June 23, 2022

Study Record Updates

• Last Update Posted (ACTUAL): September 27, 2022
• Last Update Submitted That Met QC Criteria: September 26, 2022
• Last Verified: June 1, 2022

More Information

Terms related to this study

• Keywords: Cholangiocarcinoma; Biliary tract cancer; BTC
• Additional Relevant MeSH Terms: Digestive System Diseases; Neoplasms; Neoplasms by Site; Digestive System Neoplasms; Biliary Tract Diseases; Biliary Tract Neoplasms; Antineoplastic Agents; Antineoplastic Agents, Immunological; Pembrolizumab
• Other Study ID Numbers: SNK-SIT-03

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No