A Study to Evaluate the Safety and Anti-cancer Activity of Loncastuximab Tesirine in Combination With Other Anti-cancer Agents in Participants With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma (LOTIS-7)

A Phase 1b Open-Label Study to Evaluate the Safety and Anti-cancer Activity of Loncastuximab Tesirine in Combination With Other Anti-cancer Agents in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma (LOTIS-7)

The primary objective of this study is to characterize the safety and tolerability of loncastuximab tesirine in combination with polatuzumab vedotin, glofitamab, or mosunetuzumab, and to identify the maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE) for the combinations.

Study Overview

• Status: Recruiting
• Conditions: B-Cell Non-Hodgkin Lymphoma; Refractory B-Cell Non-Hodgkin Lymphoma; Relapsed B-Cell Non-Hodgkin Lymphoma
• Intervention / Treatment: Drug: Loncastuximab Tesirine; Drug: Polatuzumab Vedotin; Drug: Glofitamab; Drug: Obinutuzumab; Drug: Mosunetuzumab

Detailed Description

This is a Phase 1b, multi-center, open-label, multi-arm study to evaluate the safety and anti-cancer activity of loncastuximab tesirine in combination with polatuzumab vedotin, glofitamab, or mosunetuzumab in participants with relapsed or refractory B-cell Non-Hodgkin Lymphoma (R/R B-NHL). The study will enroll approximately 200 participants.

Loncastuximab tesirine (ADCT-402; Zynlonta) is an antibody drug conjugate (ADC), composed of a humanized monoclonal antibody directed against human cluster of differentiation 19 (CD19) conjugated through a cathepsin-cleavable linker to a pyrrolobenzodiazepine (PBD) dimer cytotoxin. Loncastuximab tesirine has been granted by Food and Drug Administration (FDA) as accelerated approval for adult participants with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, DLBCL arising from low grade lymphoma, and high-grade B-cell lymphoma (HGBCL). In the European Union (EU), the European Commission (EC) granted conditional approval for the treatment of adult patients with relapsed or refractory DLBCL and HGBCL, after two or more lines of systemic therapy.

The study includes multiple arms in two parts, Dose Escalation part (Part 1) and Dose Expansion part (Part 2). In Part 1, for the arm of loncastuximab tesirine in combination with polatuzumab vedotin includes DLBCL, HGBCL, follicular lymphoma (FL), mantle cell lymphoma (MCL), marginal zone lymphoma (MZL), and Burkitt lymphoma (BL); for the arms of loncastuximab tesirine in combination with glofitamab or mosunetuzumab include DLBCL, HGBCL, FL, and MZL. In Part 2, participants will be treated at the dose level determined from Part 1. The Sponsor will conduct the safety monitoring and the overall supervision of the study in consultation with the Dose-Escalation Steering Committee (DESC).

For each participant, the study will include a Screening Period (of up to 28 days), a Treatment Period (cycles of 21 days), and a Follow-up Period (approximately every 12 week visits for up to two years). Participants may continue treatment for up to one year or until disease progression, unacceptable toxicity, or other discontinuation criteria, whichever occurs first.

Treatment with gemcitabine (Arm A), lenalidomide (Arm B), and umbralisib (Arm D) were removed.

• Study Type: Interventional
• Enrollment (Estimated): 200
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Contact ADC Therapeutics; Phone Number: 954-903-7994; Email: clinical.trials@adctherapeutics.com

Study Locations

• Belgium
  • Gent, Belgium, 9000
    • Recruiting
    • Universitair Ziekenhuis Gent
  • Yvoir, Belgium, B-5530
    • Recruiting
    • Centre Hospitalier Universitaire Universite Catholique de Louvain - Site Godinne
• Czechia
  • Ostrava, Czechia, 708 52
    • Recruiting
    • Fakultni nemocnice Ostrava
  • Prague, Czechia, 100 34
    • Recruiting
    • Fakultni nemocnice Kralovske Vinohrady
  • Prague, Czechia, 150 06
    • Recruiting
    • Fakultni nemocnice v Motole
  • South Moravian
    • Brno, South Moravian, Czechia, 625 00
      • Recruiting
      • Fakultni nemocnice Brno
• Italy
  • Bergamo, Italy, 24127
    • Recruiting
    • Azienda Socio Sanitaria Territoriale (ASST) Papa Giovanni XXIII
  • Bologna, Italy, 40138
    • Recruiting
    • Centro di Ricerche Cliniche - IRCCS Azienda Ospedaliero Universitaria di Bologna
  • Brescia, Italy, 25123
    • Recruiting
    • Azienda Socio Sanitaria Territoriale (ASST) degli Spedali Civili di Brescia
  • Milano, Italy, 20141
    • Recruiting
    • Istituto Europeo Di Oncologia
• Spain
  • Barcelona, Spain, 08908
    • Recruiting
    • Institut Català d'Oncologia - Hospital Duran i Reynals (ICO L'Hospitalet)
  • Madrid, Spain, 28034
    • Recruiting
    • Hospital Universitario Ramón y Cajal
  • Madrid, Spain, 28007
    • Recruiting
    • Hospital General Universitario Gregorio Maranon
  • Salamanca, Spain, 37007
    • Recruiting
    • Complejo Asistencial Universitario de Salamanca - Hospital Clínico
  • Valencia, Spain, 46026
    • Recruiting
    • Hospital Universitari I Politecnic La Fe
• United Kingdom
  • London, United Kingdom, NW1 2PG
    • Active, not recruiting
    • University College London Hospitals NHS Foundation Trust
  • Oxford, United Kingdom, OX3 7LE
    • Active, not recruiting
    • Oxford University Hospitals NHS Foundation Trust
• United States
  • Florida
    • Miami, Florida, United States, 33176
      • Recruiting
      • Miami Cancer Institute
    • Miami, Florida, United States, 33136
      • Recruiting
      • Sylvester Comprehensive Cancer Center
    • Pembroke Pines, Florida, United States, 33028
      • Recruiting
      • Memorial Cancer Institute - Memorial Hospital West
  • Georgia
    • Atlanta, Georgia, United States, 30342
      • Recruiting
      • The Blood and Marrow Transplant Group of Georgia
  • Minnesota
    • Minneapolis, Minnesota, United States, 55455
      • Recruiting
      • University of Minnesota
  • Oregon
    • Portland, Oregon, United States, 97239
      • Recruiting
      • Oregon Health and Science University
  • South Carolina
    • Charleston, South Carolina, United States, 29425
      • Recruiting
      • Hollings Cancer Center
  • South Dakota
    • Sioux Falls, South Dakota, United States, 57105
      • Withdrawn
      • Avera Cancer Institute
  • Virginia
    • Charlottesville, Virginia, United States, 22903
      • Recruiting
      • Emily Couric Clinical Cancer Center
    • Fairfax, Virginia, United States, 22031
      • Active, not recruiting
      • NEXT Virginia (Virginia Cancer Specialists)

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Male or female participant aged 18 years or older

• Pathologic diagnosis of relapsed (disease that has recurred following a response) or refractory (disease that failed to respond to prior therapy) B-NHL (2016 World Health Organization classification) who have failed, or been intolerant to any approved therapy and had received at least two systemic treatment regimens in dose-escalation part; and at least one systemic treatment regimen in dose-expansion part

  • DLBCL (including transformed diseases, but for Arms E and F, including transformed FL only)
  • HGBCL
  • FL
  • MZL
  • MCL (for Arm C only)
  • BL (for Arm C only)
• Life expectancy of at least 24 weeks according to Investigator's judgement
• Need of systemic treatment for any of the listed indications as assessed by the investigator, including indolent B-NHLs (e.g. FL and MZL)
• Measurable disease as defined by the 2014 Lugano Classification
• Availability of formalin-fixed paraffin-embedded tumor tissue block
• ECOG performance status 0 to 2
• Adequate organ function
• Women of childbearing potential (WOCBP) must agree to use a highly effective method of contraception from the time of giving informed consent until at least 10 months after the last dose of loncastuximab tesirine. Men with female partners who are of childbearing potential must agree to use a condom when sexually active or practice total abstinence from the time of giving informed consent the first dose until at least 7 months after the last dose of loncastuximab tesirine. Men must refrain from donating sperm during this same period. For the arm that includes glofitamab, WOCBP must agree to use contraceptive methods that result in a failure of <1% per year or remain abstinent (refrain from heterosexual intercourse) during the treatment period and for at least 18 months after pretreatment with obinutuzumab. For the arm that includes mosunetuzumab, WOCBP must agree to use contraceptive methods that result in a failure of <1% per year or remain abstinent (refrain from heterosexual intercourse) during the treatment period and for at least 3 months after the final dose of mosunetuzumab and tocilizumab (if applicable).

Exclusion Criteria:

• Known history of hypersensitivity resulting in treatment discontinuation to or positive serum human ADA to a CD19 antibody
• Previous therapy with loncastuximab tesirine

• Previous treatment with polatuzumab vedotin, glofitamab or mosunetuzumab (applied to relevant arm and/or cohort of the specific drug administered)

  • Participants who received previous treatment of polatuzumab vedotin containing regimen will be excluded from Arm C
  • Participants who received previous treatment of glofitamab containing regimen will be excluded from Arm E
  • Participants who received previous treatment of mosunetuzumab containing regimen will be excluded from Arm F
• Allogenic or autologous stem cell transplant within 60 days prior to start of study drug (C1 D1)
• Human immunodeficiency virus (HIV) seropositive
• Serologic evidence of chronic hepatitis B virus (HBV) infection and unable or unwilling to receive standard prophylactic antiviral therapy or with detectable HBV viral load
• Serologic evidence of hepatitis C virus (HCV) infection without completion of curative treatment or with detectable HCV viral load
• History of confirmed progressive multifocal leukoencephalopathy
• History of Stevens-Johnson syndrome, toxic epidermal necrolysis, or macrophage activation syndrome (MAS)/hemophagocytic lymphohistiocytosis (HLH)
• Lymphoma with active central nervous system (CNS) involvement at the time of screening, including leptomeningeal disease
• Clinically significant third space fluid accumulation (i.e., ascites requiring drainage or pleural effusion that is either requiring drainage or associated with shortness of breath)
• Breastfeeding or pregnant
• Significant medical comorbidities
• Major surgery, radiotherapy, chemotherapy, or other anti-neoplastic therapy, within 14 days prior to start of study drugs (C1 D1), except shorter if approved by the Sponsor
• Live vaccine within 4 weeks prior to C1D1
• Failure to recover to Grade ≤1 (Common Terminology Criteria for Adverse Events [CTCAE] version 5.0) from acute non-hematologic toxicity (Grade ≤2 alopecia) due to previous therapy prior to screening
• Active second primary malignancy other than non-melanoma skin cancers, non-metastatic prostate cancer, in situ cervical cancer, ductal or lobular carcinoma in situ of the breast, or other malignancy that the Sponsor's medical monitor and Investigator agree and document should not be exclusionary

Extra Exclusion Criteria for Arms E (includes glofitamab) and F (includes mosunetuzumab) Note: as applicable, the arm-specific exclusion criteria may supersede the general ones, such as stem cell transplant.

• Prior allogeneic stem cell transplant and solid organ transplant
• Autologous stem cell transplant within 100 days prior to C1D1
• History of CNS lymphoma or leptomeningeal infiltration
• Current or history of CNS disease, such as stroke, epilepsy, CNS vasculitis, or neurodegenerative disease
• Known active infection, reactivation of a latent infection, whether bacterial, viral, fungal, mycobacterial, or other pathogens (excluding fungal infections of nail beds), or any major episode of infection requiring hospitalization or treatment with intravenous (IV) antibiotics within four weeks prior to C1D1
• Active or history of autoimmune disease or immune deficiency, including but not limited to, myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, antiphospholipid antibody syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain Barré syndrome, or multiple sclerosis, with certain exceptions
• Prior treatment with anti-cancer/lymphoma targeted therapies (e.g., tyrosine kinase inhibitors, systemic immunotherapeutic/immunostimulating agents, including, but not limited to, cluster of differentiation 137 agonists or immune checkpoint blockade therapies, including anti-cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), anti-programmed cell death protein 1 (PD1), and anti-programmed death ligand 1 (PDL1) therapeutic antibodies, radio-immunoconjugates, ADCs, immune/cytokines and monoclonal antibodies) or treatment with systemic immunosuppressive medication (including, but not limited to, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor agents) within 4 weeks or five half-lives of the drug, whichever is shorter, prior to C1D1, or anticipation of need for systemic immunosuppressive medication during study treatment, with certain exceptions
• Prior treatment with chimeric antigen receptor T-cell therapy within 30 days prior to C1D1
• Toxicities from prior anti-cancer therapy including immunotherapy that did not resolve to ≤ Grade 1 with the exception of alopecia, endocrinopathy managed with replacement therapy and stable vitiligo
• Any history of immune-related Grade ≥3 AE with the exception of endocrinopathy managed with replacement therapy
• Ongoing corticosteroid use >25 mg/day of prednisone or equivalent within 4 weeks prior and during study treatment
• Administration of a live attenuated vaccine within 4 weeks prior to the first dose of study treatment or anticipation that such a live attenuated vaccine will be required during the study or within 5 months after last dose of study treatment

Extra Exclusion Criteria for Arm E (includes glofitamab) only.

• Known history of hypersensitivity to obinutuzumab

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Sequential Assignment
• Masking: None (Open Label)

Number of Arms

6

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Part 1 (Dose Escalation): Loncastuximab Tesirine + Polatuzumab Vedotin (Arm C); Participants will receive escalating doses (90 µg/kg to 150 µg/kg) of loncastuximab tesirine on Day (D) 1 of each cycle (where each cycle is 21 days). Participants will also receive polatuzumab vedotin at a dose of 1.8 mg/kg on D1 of each cycle, infusion will be started one hour after end of loncastuximab tesirine infusion.	Drug: Loncastuximab Tesirine; Intravenous (IV) infusion; Other Names: ADCT-402; ZYNLONTA; Drug: Polatuzumab Vedotin; IV infusion
Experimental: Part 1 (Dose Escalation): Loncastuximab Tesirine + Glofitamab (Arm E); Participants will receive escalating doses (90 µg/kg to 150 µg/kg) of loncastuximab tesirine on D2 of Cycle (C) 1 and then D1 of all other cycles (where each cycle is 21 days). Participants will also receive glofitamab 2.5 mg on C1 D8, 10 mg on C1 D15 and 30 mg for cycles 2-12 D1. In addition participants will receive obinutuzumab pre-treatment 1000 mg on C1 D1.	Drug: Loncastuximab Tesirine; Intravenous (IV) infusion; Other Names: ADCT-402; ZYNLONTA; Drug: Glofitamab; IV infusion; Drug: Obinutuzumab; IV infusion
Experimental: Part 1 (Dose Escalation): Loncastuximab Tesirine + Mosunetuzumab (Arm F); Participants will receive escalating doses (90 µg/kg to 150 µg/kg) of loncastuximab tesirine on Day (D) 1 of each cycle (where each cycle is 21 days). Participants will also receive mosunetuzumab 5 mg on C1 D1, 45 mg for C1 D8, C1 D15 and cycles 2-8 D1.	Drug: Loncastuximab Tesirine; Intravenous (IV) infusion; Other Names: ADCT-402; ZYNLONTA; Drug: Mosunetuzumab; Subcutaneous (SC) injection
Experimental: Part 2 (Dose Expansion): Loncastuximab Tesirine + Polatuzumab Vedotin (Arm C); Participants with B-NHL will receive loncastuximab tesirine in combination with polatuzumab vedotin at the maximum tolerated dose (MTD) and/or recommended dose for expansion (RDE) if favorable results of Part 1 are received.	Drug: Loncastuximab Tesirine; Intravenous (IV) infusion; Other Names: ADCT-402; ZYNLONTA; Drug: Polatuzumab Vedotin; IV infusion
Experimental: Part 2 (Dose Expansion): Loncastuximab Tesirine + Glofitamab (Arm E); Participants with B-NHL will receive loncastuximab tesirine in combination with glofitamab at the MTD and/or RDE if favorable results of Part 1 are received. In addition participants will receive obinutuzumab pre-treatment 1000 mg on C1 D1.	Drug: Loncastuximab Tesirine; Intravenous (IV) infusion; Other Names: ADCT-402; ZYNLONTA; Drug: Glofitamab; IV infusion; Drug: Obinutuzumab; IV infusion
Experimental: Part 2 (Dose Expansion): Loncastuximab Tesirine + Mosunetuzumab (Arm F); Participants with B-NHL will receive loncastuximab tesirine in combination with mosunetuzumab at the MTD and/or RDE if favorable results of Part 1 are received.	Drug: Loncastuximab Tesirine; Intravenous (IV) infusion; Other Names: ADCT-402; ZYNLONTA; Drug: Mosunetuzumab; Subcutaneous (SC) injection

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Participants Who Experience an Adverse Event (AE) Leading to Dose Delay		Up to approximately 1 year
Number of Participants Who Experience an Adverse Event (AE) Leading to Dose Interruption		Up to approximately 1 year
Number of Participants Who Experience an Adverse Event (AE) Leading to Dose Reduction		Up to approximately 1 year
Number of Participants Who Experience a Clinically Significant Change from Baseline in Vital Signs		Baseline up to approximately 1 year
Number of Participants Who Experience a Clinically Significant Change from Baseline in 12-Lead Electrocardiogram (ECG) Measurements		Baseline up to approximately 1 year
Number of Participants Who Experience a Treatment-emergent Adverse Event (TEAE)	Frequency and severity of TEAEs and treatment-emergent serious adverse events (TESAEs). TEAEs and TESAEs will be graded according to Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.	Up to approximately 2 years
Number of Participants Who Experience a Dose-Limiting Toxicity (DLT)		Day 1 to Day 21 of Cycle 1, where a cycle is 21 days
Number of Participants Who Experience a Clinically Significant Change from Baseline in Safety Laboratory Measurements		Baseline up to approximately 1 year
Number of Participants Who Experience a Clinically Significant Change from Baseline in Eastern Cooperative Oncology Group (ECOG) Performance Status	ECOG performance status will be measured on a scale from grades 0-5, where a higher grade indicates a worse outcome.	Baseline up to approximately 1 year

Secondary Outcome Measures

Outcome Measure	Time Frame
Duration of Response (DOR)	Up to approximately 2 years
Overall Response Rate (ORR)	Up to approximately 2 years
Complete Response Rate (CRR)	Up to approximately 2 years
Progression-Free Survival (PFS)	Up to approximately 2 years
Relapse-Free Survival (RFS)	Up to approximately 2 years
Overall Survival (OS)	Up to approximately 2 years
Average Concentration of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Maximum Concentration (Cmax) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Time to Maximum Concentration (Tmax) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Area Under the Concentration-Time Curve from Time Zero to the Last Quantifiable Concentration (AUClast) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Area Under the Concentration-Time Curve from Time Zero to the End of the Dosing Interval (AUCtau) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Area Under the Concentration-Time Curve from Time Zero to Infinity (AUCinf) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Apparent Terminal Elimination Half-Life (Thalf) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Apparent Clearance (CL) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Apparent Steady-State Volume of Distribution (Vss) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Accumulation Index (AI) of Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Number of Participants With Anti-Drug Antibody (ADA) Titers to Loncastuximab Tesirine	Day 1 to end of treatment (up to approximately 1 year)
Arm E Only: Number of Participants With ADA Titers to Glofitamab	Day 1 to end of treatment (up to approximately 1 year)
Arm F Only: Number of Participants With ADA Titers to Mosunetuzumab	Day 1 to end of treatment (up to approximately 1 year)

Collaborators and Investigators

• Sponsor: ADC Therapeutics S.A.

Study record dates

Study Major Dates

• Study Start (Actual): June 17, 2022
• Primary Completion (Estimated): February 12, 2025
• Study Completion (Estimated): February 10, 2026

Study Registration Dates

• First Submitted: July 12, 2021
• First Submitted That Met QC Criteria: July 12, 2021
• First Posted (Actual): July 21, 2021

Study Record Updates

• Last Update Posted (Estimated): December 20, 2023
• Last Update Submitted That Met QC Criteria: December 19, 2023
• Last Verified: December 1, 2023

More Information

Terms related to this study

• Keywords: Loncastuximab Tesirine; Refractory B-Cell Non-Hodgkin Lymphoma; B-Cell Non-Hodgkin Lymphoma; Relapsed B-Cell Non-Hodgkin Lymphoma
• Additional Relevant MeSH Terms: Immune System Diseases; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Lymphoma; Lymphoma, B-Cell; Lymphoma, Non-Hodgkin; Physiological Effects of Drugs; Antineoplastic Agents; Immunologic Factors; Antineoplastic Agents, Immunological; Immunoconjugates; Obinutuzumab; Loncastuximab tesirine; Polatuzumab vedotin
• Other Study ID Numbers: ADCT-402-105; 2021-001071-16 (EudraCT Number)

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