A Study to Evaluate Safety and Anti-Tumor Activity of Eciskafusp Alfa (RO7284755) Alone or in Combination With Atezolizumab in Participants With Advanced and/or Metastatic Solid Tumors

An Open-Label, Multicenter, Randomized, Dose-Escalation and Extension, Phase IA/IB Study to Evaluate Safety and Anti-Tumor Activity of RO7284755, A PD-1 Targeted IL-2 Variant (IL-2V) Immunocytokine, Alone or in Combination With Atezolizumab in Participants With Advanced and/or Metastatic Solid Tumors

This is an entry-into-human study and will assess the effects of eciskafusp alfa (RO7284755) as a single agent and in combination with atezolizumab in adult participants with solid tumors considered responsive to checkpoint inhibition blockade. The maximum duration in the study for each participant will be up to 28 months.

Study Overview

• Status: Recruiting
• Conditions: Solid Tumors
• Intervention / Treatment: Drug: Atezolizumab; Drug: Eciskafusp Alfa

Detailed Description

The study consists of three parts: dose-escalation of eciskafusp alfa as a single agent (Part 1), dose-escalation of eciskafusp alfa in combination with atezolizumab (Part 2), and extension of eciskafusp alfa as a single agent and/or in combination with atezolizumab (Part 3).

• Study Type: Interventional
• Enrollment (Estimated): 256
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Reference Study ID Number: BP41628 https://forpatients.roche.com/; Phone Number: 888-662-6728 (U.S. Only); Email: global-roche-genentech-trials@gene.com

Study Locations

• Belgium
  • Bruxelles, Belgium, 1200
    • Recruiting
    • Cliniques Universitaires St-Luc
  • Leuven, Belgium, 3000
    • Recruiting
    • UZ Leuven Gasthuisberg
• Canada
  • Ontario
    • Toronto, Ontario, Canada, M5G 2M9
      • Recruiting
      • Princess Margaret Cancer Center
• Denmark
  • Herlev, Denmark, 2730
    • Recruiting
    • Herlev Hospital; Afdeling for Kræftbehandling
  • København Ø, Denmark, 2100
    • Recruiting
    • Rigshospitalet; Fase 1 Enhed - Onkologi
• Netherlands
  • Amsterdam, Netherlands, 1066 CX
    • Active, not recruiting
    • NKI/AvL
  • Rotterdam, Netherlands, 3015 GD
    • Active, not recruiting
    • Erasmus MC
• Poland
  • Gda?sk, Poland, 80-214
    • Recruiting
    • Uniwersyteckie Centrum Kliniczne; Osrodek Badan Wczesnych Faz
  • Warszawa, Poland, 02-781
    • Recruiting
    • Narodowy Instytut Onkologii im. M. Sklodowskiej-Curie; Oddzial Badan Wczesnych Faz
• Spain
  • Barcelona, Spain, 08003
    • Recruiting
    • Hospital del Mar; Servicio de Oncologia
  • Barcelona, Spain, 08035
    • Recruiting
    • Vall d?Hebron Institute of Oncology (VHIO), Barcelona
  • Barcelona, Spain, 08036
    • Completed
    • Hospital Clinic Barcelona; Servicio de oncologia
  • Madrid, Spain, 28027
    • Recruiting
    • Clinica Universidad de Navarra Madrid; Servicio de Oncología
  • Madrid, Spain, 28040
    • Recruiting
    • START Madrid-FJD, Hospital Fundacion Jimenez Diaz
  • Navarra
    • Pamplona, Navarra, Spain, 31008
      • Recruiting
      • Clinica Universitaria de Navarra; Servicio de Oncologia

Participation Criteria

Eligibility Criteria

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

Description

Inclusion Criteria:

• Locally advanced/unresectable or metastatic disease
• No standard of care (SoC) (approved) treatments are available for the participant, or the participant cannot tolerate such treatments
• Measurable disease, as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1)
• Eastern Cooperative Oncology Group Performance Status 0 to 1
• Life expectancy of >=12 weeks
• Consent to provide an archival tumor tissue sample
• Adequate cardiovascular, hematological, coagulative, hepatic and renal function

Exclusion Criteria:

• Rapid disease progression or suspected hyperprogression or threat to vital organs or critical anatomical sites requiring urgent alternative medical intervention
• Untreated central nervous system (CNS) metastases
• Treated asymptomatic CNS metastases
• 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 before Cycle1 Day 1 (C1D1)
• Active or history of carcinomatous meningitis/leptomeningeal disease
• Uncontrolled tumor-related pain or symptomatic hypercalcemia
• Concurrent second malignancy
• Evidence of significant, uncontrolled concomitant diseases that could affect compliance with the protocol or interpretation of results
• Episode of significant cardiovascular/cerebrovascular acute disease within 28 days before study treatment administration
• Active or uncontrolled infections
• Known HIV infection
• Hepatitis B virus (HBV) or hepatitis C virus infection
• Adverse events related to any prior radiotherapy, chemotherapy, targeted therapy, CPI therapy or surgical procedure must have resolved to Grade <=1, except alopecia Grade 2 peripheral neuropathy, and hypothyroidism and/or hypopituitarism on a stable dosage of hormone replacement therapy
• Participants with bilateral pleural effusion
• Major surgery or significant traumatic injury < 28 days before study treatment administration or anticipation of the need for major surgery during study treatment
• Known allergy or hypersensitivity to any component of the formulations of the IMPs to be administered, including but not limited to hypersensitivity to Chinese hamster ovary cell products or other recombinant or humanized antibodies
• History of severe allergic anaphylactic reactions to chimeric, human or humanized antibodies, or fusion proteins
• Previous treatment with Interleukin-2 (IL-2)/Interleukin-5 (IL-15)-like cytokines. IL-2/IL-15 use as an adjunct treatment component for adoptive cell therapy is permitted. In Part 3, patients who have received adoptive cell therapy such as tumor-infiltrating lymphocytes (TIL) are excluded.

Study Plan

How is the study designed?

Design Details

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

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Eciskafusp Alfa as a Single Agent; Part 1: Dose-escalation of eciskafusp alfa as a single agent. eciskafusp alfa will be either an intravenous administration (IV) or subcutaneous administration (SC) in multiple-ascending doses.	Drug: Eciskafusp Alfa; Participants will be administered eciskafusp alfa in different schedules.; Other Names: RO7284755
Experimental: Eciskafusp Alfa in Combination with Atezolizumab; Part 2: Dose-escalation of eciskafusp alfa in combination with atezolizumab.	Drug: Atezolizumab; Participants will be administered 1200 mg of atezolizumab once every 3 weeks.; Other Names: Tecentriq; Drug: Eciskafusp Alfa; Participants will be administered eciskafusp alfa in different schedules.; Other Names: RO7284755
Experimental: Eciskafusp Alfa as a Single Agent and/or with Atezolizumab; Part 3: Extension of eciskafusp alfa as a single agent and/or in combination with atezolizumab.	Drug: Atezolizumab; Participants will be administered 1200 mg of atezolizumab once every 3 weeks.; Other Names: Tecentriq; Drug: Eciskafusp Alfa; Participants will be administered eciskafusp alfa in different schedules.; Other Names: RO7284755

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Percentage of Participants with Adverse Events in Part 1 and Part 2	An adverse event (AE) is any untoward medical occurrence in a participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with the treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a pharmaceutical product, whether or not considered related to the pharmaceutical product. Preexisting conditions which worsen during a study are also considered as AEs. All AE events will be graded according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.	From randomization until end of Part 1 and Part 2 (up to approximately 1.5 months)
Investigator Assessed Objective Response Rate according to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in Part 3	Objective response rate (ORR) was defined as the percentage of participants with investigator-assessed objective response of complete response (CR) or partial response (PR). PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum of diameters. CR was defined as disappearance of all target and non-target lesions and normalization of tumor marker levels (as applicable to non-target lesions).	From start of extension phase until disease progression, drug discontinuation, withdrawal or death (up to approximately 26 months)
Percentage of Participants with Dose-Limiting Toxicities in Part 1 and Part 2	A DLT is defined as a clinically significant AE (classified according to the NCI CTCAE version 5) or significant laboratory abnormality that occur during the DLT assessment periods, during Part 1 and Part 2 only, and is considered by the Investigator to be related to eciskafusp alfa or to the combination of eciskafusp alfa and atezolizumab. In Part 2, expected toxicities that are, in the opinion of the Investigator, entirely attributable to atezolizumab, will not be considered DLTs.	From randomization up to day 14 (Part 1) or day 28 (Part 2)
Recommended Dose for Extension (RDE) of Eciskafusp Alfa in Parts 1 and 2		From randomization up to day 14 (Part 1) or day 28 (Part 2)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Investigator Assessed Objective Response Rate according to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in Parts 1 and 2	ORR was defined as the percentage of participants with investigator-assessed objective response of complete response (CR) or partial response (PR). PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum of diameters. CR was defined as disappearance of all target and non-target lesions and normalization of tumor marker levels (as applicable to non-target lesions).	From randomization until end of Part 1 and Part 2 (up to approximately 1.5 months)
Percentage of Participants with Adverse Events in Part 3	An AE is any untoward medical occurrence in a participant administered a pharmaceutical product and which does not necessarily have to have a causal relationship with the treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of a pharmaceutical product, whether or not considered related to the pharmaceutical product. Preexisting conditions which worsen during a study are also considered as AEs. All AE events will be graded according to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.	From start of extension phase until disease progression, drug discontinuation, withdrawal or death (up to approximately 26 months)
Disease Control Rate in Part 3	The disease control rate was defined as proportion of participants being either responder or in 'stable disease' (SD). To classify a response as SD, measurements will have to be classified as stable (according to RECIST v1.1) at least once at a minimum of 4 weeks after study entry.	From start of extension phase until disease progression, drug discontinuation, withdrawal or death (up to approximately 26 months)
Duration of Response in Part 3	Duration of response will be calculated for 'responder' participants (i.e. best [confirmed] overall response of CR or PR) and will be defined as the time from first occurrence of a documented response until the time of documented disease progression or death (death within 30 days from last study treatment) from any cause, whichever occurs first.	From start of extension phase until disease progression, drug discontinuation, withdrawal or death (up to approximately 26 months)
Progression-free survival (PFS) in Part 3	Progression-free survival was defined as the time from first dose of study treatment to the first occurrence of documented disease progression (based on RECIST 1.1 Investigator's assessment) or death from any cause, whichever occurs first.	From start of extension phase until disease progression, drug discontinuation, withdrawal or death (up to approximately 26 months)
Percentage of Immune and Tumor Cells with Positive Programmed Cell Death-1 (PD-1) and Programmed Cell Death-Ligand 1 (PD-L1) Expression in the Tumor Microenvironment (TME)		Baseline
Percentage of Immune Cells with CD8+ PD1+ and CD8+ PD1+ TCF7+ Expression		Baseline
Blood Tumor Mutational Burden	Blood tumor mutational burden is defined as the number of genetic mutations per megabase (1,000,000 bases).	Baseline
Change from Baseline in Percentage of Immune Cell Subsets	Immune cells include NK, CD8, and Treg cells	Baseline to End of Treatment (up to approximately 28 months)
Change from Baseline in Percentage of Immune Markers	Immune markers include PD-1, PD-L1, sCD25, cytokines, etc...	Baseline to End of Treatment (up to approximately 28 months)
Change from Baseline in Antidrug Antibody (ADA) to Eciskafusp Alfa		Up to 28 months
Percentage of Partcipants with ADAs to Eciskafusp Alfa		Up to 28 months
Area Under the Curve (AUC) for Eciskafusp Alfa		Predose, C1 Days 1, 2, 3, 5, 8, 9, 10, 12, 15, 16, 17, and 19; C2 Days 1, 2, 8, 9, 10, 12, 15, and 16; C3 Days 1, 2, 3, and 8; C4 Days 1 and 2; C5 Days1, 2, and 8; and days 1 and 2 for any subsequent cycles (Up to 28 months)
Minimum Concentration (Cmin) for Eciskafusp Alfa		Predose, C1 Days 1, 2, 3, 5, 8, 9, 10, 12, 15, 16, 17, and 19; C2 Days 1, 2, 8, 9, 10, 12, 15, and 16; C3 Days 1, 2, 3, and 8; C4 Days 1 and 2; C5 Days1, 2, and 8; and days 1 and 2 for any subsequent cycles (Up to 28 months)
Maximum Concentration (Cmax) for Eciskafusp Alfa		Predose, C1 Days 1, 2, 3, 5, 8, 9, 10, 12, 15, 16, 17, and 19; C2 Days 1, 2, 8, 9, 10, 12, 15, and 16; C3 Days 1, 2, 3, and 8; C4 Days 1 and 2; C5 Days1, 2, and 8; and days 1 and 2 for any subsequent cycles (Up to 28 months)
Clearance (CL) for Eciskafusp Alfa		Predose, C1 Days 1, 2, 3, 5, 8, 9, 10, 12, 15, 16, 17, and 19; C2 Days 1, 2, 8, 9, 10, 12, 15, and 16; C3 Days 1, 2, 3, and 8; C4 Days 1 and 2; C5 Days1, 2, and 8; and days 1 and 2 for any subsequent cycles (Up to 28 months)
Volume of Distribution at Steady-State Conditions (Vss) for Eciskafusp Alfa		Predose, C1 Days 1, 2, 3, 5, 8, 9, 10, 12, 15, 16, 17, and 19; C2 Days 1, 2, 8, 9, 10, 12, 15, and 16; C3 Days 1, 2, 3, and 8; C4 Days 1 and 2; C5 Days1, 2, and 8; and days 1 and 2 for any subsequent cycles (Up to 28 months)

Collaborators and Investigators

• Sponsor: Hoffmann-La Roche
• Investigators: Study Director: Clinical Trials, Hoffmann-La Roche

Study record dates

Study Major Dates

• Study Start (Actual): May 4, 2020
• Primary Completion (Estimated): November 7, 2026
• Study Completion (Estimated): May 27, 2027

Study Registration Dates

• First Submitted: March 9, 2020
• First Submitted That Met QC Criteria: March 9, 2020
• First Posted (Actual): March 11, 2020

Study Record Updates

• Last Update Posted (Actual): April 12, 2024
• Last Update Submitted That Met QC Criteria: April 11, 2024
• Last Verified: April 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms; Molecular Mechanisms of Pharmacological Action; Antineoplastic Agents; Antineoplastic Agents, Immunological; Immune Checkpoint Inhibitors; Atezolizumab
• Other Study ID Numbers: BP41628; 2019-004022-25 (EudraCT Number); 2023-503749-76-00 (Registry Identifier: EU Trial Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: Qualified researchers may request access to individual patient level data through the clinical study data request platform (www.vivli.org). Further details on Roche's criteria for eligible studies are available here (https://vivli.org/ourmember/roche/). For further details on Roche's Global Policy on the Sharing of Clinical Information and how to request access to related clinical study documents, see here (https://www.roche.com/research_and_development/who_we_are_how_we_work/clinical_trials/our_commitment_to_data_sharing.htm).

Drug and device information, study documents

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