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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03562871
Other study ID # IO102-012 / KN-764
Secondary ID 2018-000139-28KE
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date August 22, 2018
Est. completion date April 12, 2022

Study information

Verified date April 2022
Source IO Biotech
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if IO102 combined with pembrolizumab with or without chemotherapy is safe tolerable and effective in the treatment of Non-small Cell Lung Carcinoma (NSCLC). The hypothesis is that IO102 will improve the objective response rate (ORR) in patients with metastatic NSCLC.


Recruitment information / eligibility

Status Completed
Enrollment 109
Est. completion date April 12, 2022
Est. primary completion date February 6, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Histologically or cytologically confirmed metastatic NSCLC or non squamous NSCLC - Have biomarker-positive solid tumor - Male participants of childbearing potential must agree to use an adequate method of contraception starting with the first dose of study medication through 120 days after the last dose of study medication - Female participants of childbearing potential must be willing to use an adequate method of contraception for the course of the study through 120 days after the last dose of study medication - The participant must provide written informed consent - Have measurable disease per RECIST 1.1 - Have provided a blood sample and archival tumor tissue sample or newly obtained core or excisional biopsy of a tumor lesion not previously irradiated - Eastern Cooperative Oncology Group (ECOG) Performance status of 0 or 1 - Adequate organ function Exclusion Criteria: - Prior therapy with an anti-PD-1, anti-PD-L1, or anti PD L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4, OX 40, CD137) and was discontinued from that treatment due to a Grade 3 or higher immune-related AE (irAE) - Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment - Radiotherapy within 2 weeks of start of trial treatment - Vaccination with a live vaccine within 30 days prior to the first dose of trial treatment.Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g. FluMist®) are live attenuated vaccines and are not allowed. - Is currently participating in or has participated in a trial of an investigational agent or has used an investigational device within 4 weeks prior to the first dose of trial treatment. - Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior the first dose of trial treatment. - Has a known additional malignancy that is progressing or has required active treatment within the past 2 years. - Has known active CNS metastases and/or carcinomatous meningitis. - Has severe hypersensitivity (=Grade 3) to IO102, pembrolizumab, carboplatin, pemetrexed and/or any of its excipients. - Has an active autoimmune disease that has required systemic treatment in past 2 years. - Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis. - Has an active infection requiring systemic therapy. - Has a known history of human immunodeficiency virus (HIV) infection. - Known active Hepatitis B or Hepatitis C - Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the patient's participation for the full duration of the trial, or is not in the best interest of the patient to participate, in the opinion of the treating investigator. - Has known psychiatric or substance abuse disorders that would interfere with cooperating with the requirements of the trial. - Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the trial.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
IO102
test immunotherapy
pembrolizumab (Keytruda)
anti-PD-1 immunotherapy
Drug:
Carboplatin (Carboplatin Kabi)
chemotherapy
Pemetrexed (Pemetrexed Alvogen)
chemotherapy

Locations

Country Name City State
Germany Thoraxklinik Heidelberg gGmbH Heidelberg Community Of Heidelberg
Germany PIUS Hospital Oldenburg Oldenburg
Netherlands Stichting Het Nederlands Kanker Instituut Amsterdam Community Of Amsterdam
Spain Hospital Universitario de Vall d'Hebron Barcelona Catalonia
Spain Insituto Oncologico Dr Rosell. Hospital Universitario Quiron Dexeus Barcelona Catalonia
Spain Hospital Universitari de Girona Doctor Josep Trueta Girona Catalonia
Spain Hospital Puerta del Hierro Majadahonda Madrid Community Of Madrid
Spain Hospital Universitario 12 Octubre Madrid Community Of Madrid
Spain Hospital Universitario HM Sanchinarro Madrid Community Of Madrid
Spain Hospital Universitario Ramón y Cajal Madrid Community Of Madrid
Spain Servicio de Oncología-El médico del Virgen de la Victoria Málaga Andalusia
Spain Hospital Clinico Universitario de València València Horta De València
United Kingdom Guy's Hospital London

Sponsors (2)

Lead Sponsor Collaborator
IO Biotech Merck Sharp & Dohme Corp.

Countries where clinical trial is conducted

Germany,  Netherlands,  Spain,  United Kingdom, 

References & Publications (4)

Andersen MH. Immune Regulation by Self-Recognition: Novel Possibilities for Anticancer Immunotherapy. J Natl Cancer Inst. 2015 Jun 10;107(9). pii: djv154. doi: 10.1093/jnci/djv154. Print 2015 Sep. — View Citation

Iversen TZ, Engell-Noerregaard L, Ellebaek E, Andersen R, Larsen SK, Bjoern J, Zeyher C, Gouttefangeas C, Thomsen BM, Holm B, Thor Straten P, Mellemgaard A, Andersen MH, Svane IM. Long-lasting disease stabilization in the absence of toxicity in metastatic lung cancer patients vaccinated with an epitope derived from indoleamine 2,3 dioxygenase. Clin Cancer Res. 2014 Jan 1;20(1):221-32. doi: 10.1158/1078-0432.CCR-13-1560. Epub 2013 Nov 11. — View Citation

Langer CJ, Gadgeel SM, Borghaei H, Papadimitrakopoulou VA, Patnaik A, Powell SF, Gentzler RD, Martins RG, Stevenson JP, Jalal SI, Panwalkar A, Yang JC, Gubens M, Sequist LV, Awad MM, Fiore J, Ge Y, Raftopoulos H, Gandhi L; KEYNOTE-021 investigators. Carboplatin and pemetrexed with or without pembrolizumab for advanced, non-squamous non-small-cell lung cancer: a randomised, phase 2 cohort of the open-label KEYNOTE-021 study. Lancet Oncol. 2016 Nov;17(11):1497-1508. doi: 10.1016/S1470-2045(16)30498-3. Epub 2016 Oct 10. — View Citation

Reck M, Rodríguez-Abreu D, Robinson AG, Hui R, Csoszi T, Fülöp A, Gottfried M, Peled N, Tafreshi A, Cuffe S, O'Brien M, Rao S, Hotta K, Leiby MA, Lubiniecki GM, Shentu Y, Rangwala R, Brahmer JR; KEYNOTE-024 Investigators. Pembrolizumab versus Chemotherapy for PD-L1-Positive Non-Small-Cell Lung Cancer. N Engl J Med. 2016 Nov 10;375(19):1823-1833. Epub 2016 Oct 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Phase 1 (safety run-in) Dose Limiting Toxicity graded per Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 One cycle i.e. 3 weeks
Primary Phase 2 (efficacy) Objective Response Rate (ORR) evaluated by RECIST 1.1 and defined as the rate of complete response (CR) + partial response (PR) From date of randomization until date of death from any cause, withdrawal of consent or loss to follow up whichever came first, assessed for up to 35 cycles (2 years)
Secondary ORR by baseline PD-L1 expression From date of randomization until date of death from any cause, withdrawal of consent or loss to follow up whichever came first, assessed for up to 35 cycles (2 years)
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