A Study of ASP2998 Given by Itself and Given With Standard Therapies in People With Solid Tumors

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorAstellas Pharma Global Development, Inc.

About this trial

Specific proteins found in tumors help the tumors spread and grow. People with solid tumors often have a protein called TROP2 in their tumor. ASP2998 is being developed to attach to TROP2 and then attack the tumor cells in people with solid tumors. ASP2998 will either be given by itself, or given together with one or more of standard cancer treatments pembrolizumab, carboplatin, and enfortumab vedotin.

This is an early development study to collect information about ASP2998 in people with solid tumors. In this study ASP2998 will be given to humans for the first time. Early development studies are mostly about safety, but also to find the most suitable dose. Other aims are to check if ASP2998 shows signs of reducing tumor growth, to learn how the body processes ASP2998, and to check if there are changes either in the TROP2 protein or in the immune system.

The main aim of the study is to check the safety of ASP2998 when given by itself and given with the standard cancer treatments, and how well it is tolerated.

People in this study will be adults with locally advanced, unresectable or metastatic solid tumors. Locally advanced means the cancer has spread to nearby tissue. Unresectable means the cancer cannot be removed by surgery. Metastatic means the cancer has spread to other parts of the body. People's cancer came back or became worse after previous treatment or they couldn't receive treatment. Some people who had previously refused treatment may be able to take part. This will depend on which study treatment they receive.

People will either have cancer in the bladder lining (urothelial cancer), non-small cell lung cancer (NSCLC), gastric cancer or cancer where the food pipe joins the stomach (gastroesophageal cancer, or GEJ), or certain types of breast cancer.

People cannot take part if the cancer cells have spread to the thin tissue covering the brain and spinal cord (leptomeningeal disease), have symptoms of cancer in the brain or nervous system, or need medicines to suppress their immune system.

In this study, ASP2998 will be given to humans for the first time. ASP2998 will either be given by itself, or given together with one or more of standard cancer treatments pembrolizumab, carboplatin and enfortumab vedotin. The standard cancer treatment given will depend on which cancer people have.

The study will have 2 parts.

In Part 1, different small groups of people will receive lower to higher doses of ASP2998 given by itself or together with one or more of the standard cancer treatments. Any medical problems will be recorded for each dose. This is done to find suitable doses of ASP2998 to use in Part 2.

In Part 2, other different small groups will receive suitable doses of ASP2998 worked out from Part 1. ASP2998 will either be given by itself or given together with one or more of the standard cancer treatments. This part will also check how each type of cancer responds to ASP2998 when given by itself or together with the standard cancer treatments.

In both parts of the study, safety checks will be done at each visit, and the doctors will continue to check for medical problems throughout the study. ASP2998 will be given slowly through a tube into a vein (infusion). People will continue to receive ASP2998 until their cancer gets worse, they can't tolerate ASP2998, they start other cancer treatment, they or the doctor decides the person should stop receiving ASP2998.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participant has a confirmed diagnosis of locally advanced unresectable or metastatic solid tumors.

Participant has progressed on, is ineligible for, or has refused all available standard therapies (no limit to the number of prior treatment regimens).

Prior exposure to TROP2, stimulator of interferon genes (STING) agonist or topoisomerase I (TopI) directed therapy is allowed.

Participant must have one of the following malignancies: Urothelial carcinoma, NSCLC (nonsquamous cell histology), Gastric/ gastroesophageal junction (GEJ) cancer, Breast cancer (human epidermal growth factor receptor 2 [HER2]-negative; local testing for HER2 status is acceptable).

Disqualifiers

Participant weighs < 40 kg during screening.

Participant has known active central nervous system (CNS) metastases. NOTE: A participant with CNS metastases that have been treated with surgery and/or radiation therapy, who is no longer taking pharmacologic doses of glucocorticoids and is neurologically stable, is eligible. Prophylactic use of anticonvulsants is permitted.

Any history of recurrent Grade 3 AEs/ immune-related AEs (irAEs) or history of Grade 4 irAEs related to prior anticancer therapy.

Recurrent Grade 3 or Grade 4 toxicities related to prior anticancer therapy not improved to Grade ≤ 1 or baseline per National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v5.0 or higher at least 28 days prior to initiating screening. NOTE: Participant with chronic, stable Grade ≤ 2 toxicities is eligible if the toxicity has not worsened beyond Grade 2 for at least 3 months prior to C1D1 and is managed with standard of care treatment, and is considered by the investigator to be related to prior anticancer therapy. However, a participant who meets other exclusion criteria will be excluded from the study regardless of the above provisions.

Trial design

Design model

Sequential

Treatments tested in this trial

  • ASP2998

    Drug

    Intravenous infusion

  • Pembrolizumab

    Drug

    Intravenous infusion

  • Enfortumab Vedotin

    Drug

    Intravenous infusion

  • Carboplatin

    Drug

    Intravenous infusion

Treatment groups

428 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Group A: ASP2998 Dose EscalationExperimental treatment 1 intervention
Group B: ASP2998 Dose ExpansionExperimental treatment 1 intervention
Group C: ASP2998 Monotherapy Dose Escalation (Tumor Specific)Experimental treatment 1 intervention
Group D: ASP2998 Monotherapy Dose Expansion (Tumor Specific)Experimental treatment 1 intervention
Group E: ASP2998 Combination Therapy Dose Escalation (Tumor Specific)Experimental treatment 4 interventions
Group F: ASP2998 Combination Therapy Dose Expansion (Tumor Specific)Experimental treatment 4 interventions

Trial outcomes

Primary outcomes

1

Number of Participants with Dose Limiting Toxicities (DLTs)

A DLT is defined as any event meeting the DLT criteria occurring within 21 days of first dose on Cycle 1 Day 1 (C1D1) that cannot clearly be attributed to a cause other than ASP2998 administered in monotherapy or in combination with standard treatments.

Time frame
Up to 21 days
2

Number of Participants with Treatment-Emergent Adverse Events (TEAEs)

An AE is any untoward medical occurrence in a patient or clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. NOTE: An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom or disease (new or exacerbated) temporally associated with the use of study intervention. This includes events related to the comparator, if applicable, and events related to the (study) procedures. A TEAE is an AE with onset at any time from first dosing until last scheduled procedure.

Time frame
Up to 21 Months
3

Number of participants with laboratory value abnormalities and/or adverse events (AEs)

Number of participants with potentially clinically significant laboratory values.

Time frame
Up to 21 months
4

Number of participants with vital sign abnormalities and/or AEs

Number of participants with potentially clinically significant vital sign values.

Time frame
Up to 19 months

Secondary outcomes

1

Objective Response Rate (ORR) of ASP2998 per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1

ORR is defined as the proportion of participants whose best overall response is rated as Complete Response (CR) or Partial Response (PR) per RECIST v1.1 as assessed by the investigator.

Time frame
Up to 27 months
2

Duration of Response (DOR) of ASP2998 per RECIST v1.1

DOR is defined as the time from the date of first documented response (CR or PR that is subsequently confirmed) to the date of first documented progressive disease (PD) per RECIST v1.1 as assessed by the investigator or death due to any cause, whichever occurs first.

Time frame
Up to 27 months
3

Disease Control Rate (DCR) of ASP2998 per RECIST v1.1

DCR is defined as the proportion of participants whose best overall response is rated as CR, PR or stable disease (SD) per RECIST v1.1 as assessed by the investigator.

Time frame
Up to 27 months
4

Progression Free Survival (PFS) per RECIST v1.1

PFS is defined as the time from the first dose of study intervention until the date of documented PD per RECIST v1.1 as assessed by the investigator or until death for any cause, whichever comes first.

Time frame
Up to 27 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.