Dose Escalation and Expansion Study of GSK3359609 in Participants With Selected Advanced Solid Tumors (INDUCE-1)

Neoplasms Clinical Trial

Official title:

A Phase I Open Label Study of GSK3359609 Administered Alone and in Combination With Anticancer Agents in Subjects With Selected Advanced Solid Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02723955
• Other study ID #: 204691
• Secondary ID: 2016-000148-32
• Status: Completed
• Phase: Phase 1
• Start date: June 23, 2016
• Est. completion date: July 5, 2023

Study information

• Verified date: February 2024
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

GSK3359609 is an anti-Inducible T cell Co-Stimulator (ICOS) receptor agonist antibody intended for the treatment of cancers of different histology. This is a first-time-in-human (FTIH), open-label, multicenter study designed to investigate the safety, pharmacology, and preliminary antitumor activity in participants with selected, advanced or recurrent solid tumors with the aim to establish recommended dose(s) of GSK3359609 for further exploration as monotherapy and in combination with pembrolizumab or chemotherapy regimens. The study is comprised of two primary parts, each composed of two phases: Part 1: GSK3359609 monotherapy with Part 1A as dose escalation phase and Part 1B as cohort expansion phase; Part 2: GSK3359609 combination therapy with Part 2A pembrolizumab or GSK3174998 or dostarlimab or dostarlimab plus cobolimab or Bintrafusp alfa combination dose escalation phase and Part 2B expansion phase with pembrolizumab. Part 2A GSK3359609 combinations with chemotherapy will only consist of safety run-in cohorts. Each part and phase of the study includes a screening period, a treatment period, and a follow-up period. The primary objective of the study is to determine the safety, tolerability, maximum tolerated dose or the maximum administered dose of GSK3359609 alone or in combination.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 829
• Est. completion date: July 5, 2023
• Est. primary completion date: July 5, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

• Capable of giving signed, written informed consent.

• Male or female, age >=18 years (at the time consent is obtained).

• Histological or cytological documentation of an invasive malignancy that was diagnosed as locally advanced/metastatic or relapsed/refractory and is of one of the following tumor types: bladder/urothelial cancer of the upper and lower urinary tract; cervical; colorectal (includes appendix); esophagus, squamous cell; head and neck carcinoma; melanoma; malignant pleural mesothelioma (MPM); non-small-cell lung cancer (NSCLC), prostate; Microsatellite Instability-High/deficient mismatch repair (MSI-H/dMMR) tumor (Part 1B and Part 2B) and Human Papilloma Virus (HPV)-positive or Epstein-Barr (EBV)-positive tumor (Part 1B and Part 2B).

• Disease that has progressed after standard therapy for the specific tumor type, or for which standard therapy has proven to be ineffective, intolerable, or is considered inappropriate, or if no further standard therapy exists; exceptions are in these tumor types in which pembrolizumab single agent may be a standard: NSCLC, head and neck squamous cell cancer (HNSCC), bladder/urothelial cancer, MSI-H/dMMR cancers and melanoma and cervical cancer. In Part 2B pembrolizumab combination expansion cohorts, prior treatment with anti-Programmed cell death protein 1(PD-1)/ Ligand-1 (L1) may not be required. 1) Participants must not have received more than 5 prior lines of therapy for advanced disease including both standards of care and investigational therapies. 2) Participants who received prior PD-1/L1 therapy must fulfill the following requirements (Part 1B [except PK/PD cohort]/ Part 2B):a) Have achieved a CR, PR or SD and subsequently had disease progression while still on PD-1/L1 therapy; b) Have received at least 2 doses of an approved PD-1/L1 inhibitor (by any regulatory authority), c) Have demonstrated disease progression as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 within 18 weeks from the last dose of the PD-1/L1 inhibitor. The initial evidence of disease progression is to be confirmed by a second assessment no less than four weeks from the date of the first documented Progressive Disease (PD) (the confirmatory scan could be the Baseline eligibility scan for this study). 3) In Part 2A 5-fluorouracil (FU)/platinum combination with GSK3359609 and pembrolizumab cohort, participants must not have received prior systemic therapy administered in the recurrent or metastatic setting (with the exception of systemic therapy given as part of multimodal treatment for locally advanced disease).

• Archival tumor tissue obtained at any time from the initial diagnosis to study entry; a fresh tumor biopsy using a procedure that is safe for the participant on a lesion not previously irradiated unless lesion progressed will be required if archival tissue is unavailable.

• Agree to undergo a pre-treatment and on treatment biopsy and have disease amenable to biopsy required in pharmacokinetic (PK) / pharmacodynamics (PD), dose randomized HNSCC, Melanoma dose expansion and Biomarker cohorts..

• Measurable disease per RECIST version 1.1. Palpable lesions that are not measurable by radiographic or photographic evaluations may not be utilized as the only measurable lesion. Any measurable lesion biopsied at Screening cannot be followed as a target/index lesion unless agreed upon by GlaxoSmithKline (GSK).

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1.

• Life expectancy of at least 12 weeks.

• Adequate organ function.

• QT interval corrected for heart rate according to Fridericia's formula (QTcF) <450 milliseconds (msec) or QTcF <480 msec for participants with bundle branch block.

• A female participant is eligible to participate if she is not pregnant (as confirmed by a negative serum beta-human chorionic gonadotrophin [beta-hCG] test in females of reproductive potential), and not lactating or reproductive potential agrees to follow one of the options listed in protocol from 30 days prior to the first dose of study medication and until 120 days after the last dose of study treatment.

• Male participants with female partners of child bearing potential must agree to use one of the methods of contraception specified in protocol from time of first dose of study treatment until 120 days after the last dose of study treatment.

• Documented HPV/ EBV-positive tumor as determined by a local laboratory for Part 1B and Part 2B pembrolizumab combination viral-positive expansion cohorts only.

• Documented MSI-H or dMMR-positive tumor as determined by local laboratory for Part 1B and Part 2B pembrolizumab combination MSI-H/dMMR expansion cohorts only.

• ICOS expression result using an analytically validated immunohistochemistry (IHC) assay by central laboratory for Part 1B biomarker cohort only.

• Gene expression (GEX) result using an analytically validated method by central laboratory (Part 1B Biomarker Cohort only).

• PD-L1 combined positive score (CPS) <1 using the Food and Drug Administration (FDA) approved PD-L1 IHC 22C3 pharmdx assay by central laboratory testing for Part 2B HNSCC PD-L1 CPS <1 Cohort. Documented test result from FDA approved PD-L1 IHC 22C3 pharmDx assay in local laboratory, if available, may be accepted in lieu of the central laboratory test result.

Exclusion Criteria

• Prior treatment with the following therapies:

• Anticancer therapy within 30 days or 5 half-lives of the drug, whichever is shorter. At least 14 days must have elapsed between the last dose of prior anticancer agent and the first dose of study drug is administered.

• Part 2B (GSK3359609/pembrolizumab combination): prior pembrolizumab washout is not required.

• Prior radiation therapy: permissible if at least one non-irradiated measurable lesion is available for assessment according to RECIST version 1.1 or if a solitary measurable lesion was irradiated, objective progression is documented. A wash out of at least two weeks before start of study drug for radiation of any intended use to the extremities for bone metastases and 4 weeks for radiation to the chest, brain, or visceral organs is required. • Investigational therapy within 30 days or 5 half-lives of the investigational product (whichever is shorter). At least 14 days must have elapsed between the last dose of investigational agent and the first dose of study drug is administered.

• Prior allogeneic or autologous bone marrow transplantation or other solid organ transplantation.

• Toxicity from previous anticancer treatment

• Invasive malignancy or history of invasive malignancy other than disease under study within the last two years except: Any other invasive malignancy for which the participant was definitively treated, has been disease-free for <=2 years and in the opinion of the principal investigator and GSK Medical Monitor will not affect the evaluation of the effects of the study treatment on the currently targeted malignancy, may be included in this clinical trial; and curatively treated non-melanoma skin cancer.

• Central nervous system (CNS) metastases, with the following exception: • Participants who have previously-treated CNS metastases, are asymptomatic, and have no requirement for steroids at least 14 days prior to first dose of study drug. Participants with carcinomatous meningitis or leptomeningeal spread are excluded regardless of clinical stability.

• Received transfusion of blood products (including platelets or red blood cells) or administration of colony stimulating factors (including granulocyte colony-stimulating factor [G-CSF], granulocyte-macrophage colony-stimulating factor, recombinant erythropoietin) within 14 days prior to the first dose of GSK3359609.

• Major surgery <=4 weeks before the first dose of study treatment. Participants must have also fully recovered from any surgery (major or minor) and/or its complications before initiating study treatment.

• Active autoimmune disease that has required systemic treatment within the last two years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.

• Concurrent medical condition requiring the use of systemic immunosuppressive medications within 7 days before the first dose of study treatment. Physiologic doses of corticosteroids for treatment of endocrinopathies or steroids with minimal systemic absorption, including topical, inhaled, or intranasal corticosteroids may be continued if the participant is on a stable dose.

• Condition requiring treatment with strong inhibitors/inducers of cytochrome p (CYP) 450 3A4 within 7 days prior to first dose of chemotherapy (requirement applies to participants enrolled to Part 2 chemotherapy combination with docetaxel).

• Active infection requiring systemic therapy, known human immunodeficiency virus infection, or positive test for hepatitis B active infection or hepatitis C active infection.

• Current active liver or biliary disease (with the exception of Gilbert's syndrome or asymptomatic gallstones, liver metastases, or otherwise stable chronic liver disease per investigator assessment).

• Recent history (within the past 6 months) of acute diverticulitis, inflammatory bowel disease, intra-abdominal abscess, or gastrointestinal obstruction that required surgery.

• Receipt of any live vaccine within 4 weeks prior to first dose of study treatment.

• Recent history of allergen desensitization therapy within 4 weeks of starting study treatment.

• History of severe hypersensitivity to monoclonal antibodies or to the chemotherapies under investigation including any ingredient used in the formulation.

• History or evidence of cardiac abnormalities.

• History of (current and past) idiopathic pulmonary fibrosis, pneumonitis (for past pneumonitis exclusion only if steroids were required for treatment), interstitial lung disease, or organizing pneumonia. Note: post-radiation changes in the lung related to prior radiotherapy and/or asymptomatic radiation-induced pneumonitis not requiring treatment may be permitted if agreed by the investigator and Medical Monitor.

• Recent history (within 6 months) of uncontrolled symptomatic ascites or pleural effusions.

• Any serious and/or unstable pre-existing medical, psychiatric disorder, or other condition that could interfere with the participant's safety, obtaining informed consent, or compliance to the study procedures.

Related Conditions & MeSH terms

• Neoplasms

Intervention

Drug:
• feladilimab (GSK3359609)

• GSK3174998

• Pembrolizumab

• Docetaxel

• Pemetrexed

• Paclitaxel plus Carboplatin

• Gemcitabine plus Carboplatin

• Fluorouracil (5-FU) plus carboplatin or cisplatin

• Dostarlimab

• Cobolimab

• Bintrafusp alfa

Locations

Country	Name	City	State
Australia	GSK Investigational Site	Heidelberg	Victoria
Australia	GSK Investigational Site	Melbourne	Victoria
Australia	GSK Investigational Site	Nedlands	Western Australia
Canada	GSK Investigational Site	Toronto	Ontario
China	GSK Investigational Site	Shnghai
France	GSK Investigational Site	Bordeaux Cedex
France	GSK Investigational Site	Lyon cedex 08
France	GSK Investigational Site	Paris
France	GSK Investigational Site	Villejuif cedex
Italy	GSK Investigational Site	Siena	Toscana
Japan	GSK Investigational Site	Chiba
Japan	GSK Investigational Site	Osaka
Japan	GSK Investigational Site	Tokyo
Netherlands	GSK Investigational Site	Amsterdam
Spain	GSK Investigational Site	Barcelona
Spain	GSK Investigational Site	Barcelona
Spain	GSK Investigational Site	Madrid
Spain	GSK Investigational Site	Málaga
Spain	GSK Investigational Site	Sevilla
United States	GSK Investigational Site	Duarte	California
United States	GSK Investigational Site	Los Angeles	California
United States	GSK Investigational Site	Nashville	Tennessee
United States	GSK Investigational Site	Nashville	Tennessee
United States	GSK Investigational Site	New York	New York
United States	GSK Investigational Site	New York	New York
United States	GSK Investigational Site	Oklahoma City	Oklahoma
United States	GSK Investigational Site	Philadelphia	Pennsylvania
United States	GSK Investigational Site	Sarasota	Florida

Sponsors (2)

Lead Sponsor	Collaborator
GlaxoSmithKline	Merck Sharp & Dohme LLC

Countries where clinical trial is conducted

United States,  Australia,  Canada,  China,  France,  Italy,  Japan,  Netherlands,  Spain, 

References & Publications (1)

Turner DC, Wada R, Zhou H, Wang X, de Greef R, Valiathan C, Zhang L, Zhang N, Kuchimanchi M, Chen TT, Ballas M, Visser SAG. Model-based meta-analysis of non-small cell lung cancer with standard of care PD-1 inhibitors and chemotherapy for early development decision making. CPT Pharmacometrics Syst Pharmacol. 2023 Nov;12(11):1751-1763. doi: 10.1002/psp4.12917. Epub 2023 Jan 31. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Parts 1 and 2: Number of participants with any months adverse event(s) (AE) and serious adverse event(s) (SAE)	AEs and SAEs will be collected.	Up to 27 months
Primary	Parts 1 and 2: Number of participants with dose limiting toxicity (DLT)	Number of participants with DLTs will be assessed.	Up to 28 days
Primary	Parts 1 and 2: Number of participants with clinically significant changes in laboratory parameters and vital signs	Number of participants with clinically significant changes in laboratory parameters and vital signs will be assessed.	Up to 24 months
Primary	Parts 1 and 2: Number of participants requiring dose modifications	All dose modifications due to any reason(s) will be recorded.	Up to 24 months
Secondary	Parts 1 and 2: Disease control rate (DCR)	DCR is defined as the percentage of participants with a confirmed complete response (CR) + partial response (PR) at any time, plus stable disease (SD) >=18 weeks.	Up to 27 months
Secondary	Parts 1 and 2: Overall survival (OS)	OS is defined as time from the date of first dose of study treatment to the date of death due to any cause.	Up to 4 years
Secondary	Parts 1 and 2: Progression-free survival (PFS)	PFS is defined as time from the date of first dose of study treatment to the date of disease progression according to clinical or radiographic assessment or death due to any cause, whichever occurs earliest.	Up to 27 months
Secondary	Parts 1 and 2: Time to overall response (TTR)	TTR will be summarized for participants with a confirmed CR or PR and is defined as the time from date of first dose of study treatment to date of first documented confirmed CR or PR.	Up to 27 months
Secondary	Parts 1 and 2: Duration of response (DOR)	DOR will be summarized for participants with a confirmed CR or PR and is defined as the time from date of initial confirmed response to the date of disease progression or death due to any cause.	Up to 27 months
Secondary	Parts 1 and 2: Overall response rate (ORR)	ORR is defined as the percentage of participants with a best overall confirmed CR or a PR at any time as per disease-specific criteria.	Up to 27 months
Secondary	Parts 1 and 2: Maximum observed plasma concentration (Cmax) and minimum observed plasma concentration (Cmin) of GSK3359609	Blood samples will be collected for the concentrations of GSK3359609.	Up to 27 months
Secondary	Parts 1 and 2: Area under the concentration-time curve over the dosing interval (AUC[0-tau]) of GSK3359609 in plasma	Blood samples will be collected for the concentrations of GSK3359609.	Up to 27 months
Secondary	Parts 1 and 2: Number of participants with positive results in Anti-drug antibody (ADA) test by GSK3359609 dose level	Blood samples will be collected up to 27 months for ADA test.	Up to 27 months
Secondary	Part 1 and 2: Number of participants with positive results in GSK3359609	Blood samples will be collected up to 27 months for immunogenicity.	Up to 27 months
Secondary	Part 2: Number of participants with DLT following administration of GSK3359609 in combination with chemotherapies	Number of participants with DLTs will be assessed.	Up to 28 days
Secondary	Part 2: Cmax and Cmin of GSK3174998	Blood samples will be collected for the concentrations of GSK3174998.	Up to 24 months
Secondary	Part 2: AUC(0-tau) of GSK3174998	Blood samples will be collected for the concentrations of GSK3174998.	Up to 24months
Secondary	Part 2: Cmax and Cmin of Pembrolizumab	Blood samples will be collected for the concentrations of Pembrolizumab.	Up to 27 months
Secondary	Part 2: AUC(0-tau) of Pembrolizumab	Blood samples will be collected for the concentrations of Pembrolizumab.	Up to 27 months
Secondary	Part 2: Number of participants with positive results in ADA test by GSK3359609 in combination with pembrolizumab or GSK3174998 dose level	Blood samples will be collected up to 27 months for ADA test.	Up to 27 months
Secondary	Part 2: Number of participants with positive results in Pembrolizumab	Blood samples will be collected up to 27 months for immunogenicity.	Up to 27 months
Secondary	Part 2: Number of participants with positive results in GSK3174998	Blood samples will be collected up to 27 months for immunogenicity.	Up to 27 months
Secondary	Part 2: Cmax and Cmin of GSK3359609 combination with chemotherapies	Blood samples will be collected for the concentrations of GSK3359606 in combination with chemotherapies.	Up to 27 months
Secondary	Part 2: Number of participants with positive results in ADA test by GSK3359609 combination with chemotherapies dose level	Blood samples will be collected up to 27 months for ADA test.	Up to 27 months
Secondary	Part 2: Cmax and Cmin of dostarlimab	Blood samples will be collected for the concentrations of dostarlimab.	Up to 27 months
Secondary	Part 2: AUC(0-tau) of dostarlimab	Blood samples will be collected for the concentrations of dostarlimab.	Up to 27 months
Secondary	Part 2: Cmax and Cmin of cobolimab	Blood samples will be collected for the concentrations of cobolimab.	Up to 27 months
Secondary	Part 2: AUC(0-tau) of cobolimab	Blood samples will be collected for the concentrations of cobolimab.	Up to 27 months
Secondary	Part 2: Cmax and Cmin of bintrafusp alfa	Blood samples will be collected for the concentrations of bintrafusp alfa.	Up to 27 months
Secondary	Part 2: AUC(0-tau) of bintrafusp alfa	Blood samples will be collected for the concentrations of bintrafusp alfa.	Up to 27 months