First-in-human Trial of EGL-001 in Patients with Selected Advanced And/or Metastatic Solid Tumors

NCT ID: NCT06622486

Last Updated: 2024-11-07

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-09-27
• Study Completion Date: 2027-01-23

Brief Summary

This multicenter, open-label, first-in-human, Phase 1/2 study consists of a Part 1 (Phase 1) open-label dose escalation of EGL-001 administered as a single agent and in combination with an anti-PD(L)-1 treatment, followed by a Part 2 (Phase 2) open-label dose expansion of EGL-001 administered at the RP2D in patients with recurrent and/or metastatic solid tumors as monotherapy and/or combination therapy with anti-PD(L)-1.

Detailed Description

In approximately 4 centers in France and 4 centers in Spain, 30 to 50 patients will be included in the dose escalation Part 1 of the trial. Number of participating countries and sites as well as patients will be defined based on Part 1 for Part 2 dose expansion phase.

Conditions

Solid Tumor, Adult

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Monotherapy EGL-001 Dose Level 1

EGL-001 Dose Level 1

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Monotherapy EGL-001 Dose Level 2

EGL-001 Dose Level 2

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Monotherapy EGL-001 Dose Level 3

EGL-001 Dose Level 3

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Monotherapy EGL-001 Dose Level 4

EGL-001 Dose Level 4

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Monotherapy EGL-001 Dose Level 5

EGL-001 Dose Level 5

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Monotherapy EGL-001 Dose Level 6

EGL-001 Dose Level 6

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Monotherapy EGL-001 Dose Level 7

EGL-001 Dose Level 7

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Combination therapy with EGL-001 dose Level x

EGL-001 Dose Level x in combination with anti-PDL1

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Combination therapy with EGL-001 dose Level y

EGL-001 Dose Level y in combination with anti-PDL1

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Combination therapy with EGL-001 dose Level z

EGL-001 Dose Level z in combination with anti-PDL1

Group Type: EXPERIMENTAL

EGL-001

Intervention Type: DRUG

IV administration

Interventions

EGL-001

IV administration

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Signed written informed consent

2. Female or male patients, aged at least 18 years

3. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

4. Life expectancy of at least 3 months as assessed by the investigator

5. Patients with confirmed locally advanced, unresectable, or metastatic solid tumors who have been previously treated with SoC and are no longer eligible for other therapies

6. Patients who have been treated with an ICI treatment as monotherapy or in combination as SoC

7. Have recovered from previous treatment

8. At least 1 measurable lesion according to RECIST Version 1.1

9. Adequate hematological, hepatic, and renal functions

10. Negative blood pregnancy test at screening for women of childbearing potential

11. Highly effective contraception during the study period and for 6 months after the last study treatment administration for WOCBP, and for male patients who are sexually active with WOCBP. Highly effective contraception methods are defined as:

• Hormonal methods of contraception including combined oral contraceptive pills, vaginal ring, injectable, implants, intrauterine devices such as Mirena and nonhormonal intrauterine devices such as ParaGard for WOCBP patients or male patients' WOCBP partners
• Tubal ligation
• Vasectomy

In addition to highly effective contraception, participating male patients:

• Must use a condom during the study period and for 3 months after the last study treatment administration when engaging in any activity that allows for exposure to ejaculate
• Must refrain from donating sperm

12. Must agree to abstain from donating blood while taking study drug and for 3 months following discontinuation of study treatment

13. Able to understand the character and individual consequences of clinical trial

Exclusion Criteria

1. Patients with central nervous system metastases and/or leptomeningeal carcinomatosis with some exceptions

2. Patients with active or a documented history of autoimmune disease, immune deficiency or syndrome that required systemic corticoids (except the allowed dose) or immunosuppressive medications

3. Patients who received a previous ICI like anti-PD(L)-1 or an agent directed to another stimulatory or co-inhibitory T-cell receptor and was discontinued from that treatment due to toxicity

4. Patients under chronic treatment with systemic corticosteroids or other immunosuppressive drugs for a period of at least 4 weeks and whose treatment was not stopped 2 weeks prior to the first study treatment, with exceptions. Steroids with no or minimal systemic effect (topical, inhalation) are allowed

5. Patients with history of or current interstitial lung disease or fibrosis, and patients with pneumonitis

6. Other active malignancy requiring active intervention

7. Patients with previous malignancies other than the target malignancy to be investigated in this trial, unless a complete remission was achieved and no additional therapy is required during the study period

8. Patient with any organ transplantation, including allogeneic stem cell transplantation

9. Known severe hypersensitivity reactions to monoclonal antibodies, any history of anaphylaxis, or uncontrolled asthma

10. Any known allergy or severe reaction to any component of anti-CTLA-4 or anti-PD(L)-1 drug product

11. Significant chronic or acute infections requiring systemic therapy including SARS-CoV-2 (COVID-19) PCR positive testing

12. Clinically significant active cardiovascular disease

13. Any other medical conditions or psychological disorders that would increase the safety risk to the patient or interfere with participation of the patient or the evaluation of the clinical study in the opinion of the investigator

14. Pregnant, breastfeeding, or expecting to conceive or father children within the projected duration of the trial

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Egle Therapeutics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pejvack Motlagh, MD

Role: STUDY_DIRECTOR

Egle Therapeutics

Locations

Centr Georges Francois Leclerc

Dijon, , France

Site Status: NOT_YET_RECRUITING

Institut Regional Du Cancer De Montpellier

Montpellier, , France

Site Status: RECRUITING

Institut Curie

Paris, , France

Site Status: RECRUITING

Institut Gustave Roussy

Paris, , France

Site Status: NOT_YET_RECRUITING

Hospital Universitari Vall D Hebron

Barcelona, , Spain

Site Status: NOT_YET_RECRUITING

Hospital Universitario Fundacion Jimenez Diaz

Madrid, , Spain

Site Status: NOT_YET_RECRUITING

Clinica Universidad De Navarra

Pamplona, , Spain

Site Status: NOT_YET_RECRUITING

Hospital Clinico Universitario De Valencia

Valencia, , Spain

Site Status: RECRUITING

Countries

France; Spain

Central Contacts

Pejvack Motlagh, MD

Role: CONTACT

contact@egle-tx.com

33660462343

Facility Contacts

Alice HERVIEU, MD

Role: primary

ahervieu@cgfl.fr

+33380737506

Diego TOSI, MD

Role: primary

diego.tosi@icm.unicancer.fr

+33467612304

Christophe LE TOURNEAU, MD

Role: primary

christophe.letourneau@curie.fr

+33144324086

Aurélien MARABELLE, MD

Role: primary

aurelien.marabelle@gustaveroussy.fr

+33142115592

Elena GARRALDA CABANAS, MD

Role: primary

egarralda@vhio.net

+34932746085

Victor MORENO GARCIA, MD

Role: primary

victor.moreno@startmadrid.com

+34915504800

Ana LANDA MAGDALENA, MD

Role: primary

alandam@unav.es

+34948255400

Valentina GAMBARDELLA, MD

Role: primary

Valen.gambardella@gmail.com

+34691135106

Other Identifiers

2024-512921-10-00

Identifier Type: CTIS

Identifier Source: secondary_id

EGL-121

Identifier Type: -

Identifier Source: org_study_id