Debio 0123 in Combination With Carboplatin and Etoposide in Adult Participants With Small Cell Lung Cancer That Recurred or Progressed After Previous Standard Platinum-Based Therapy

Sponsor

Debiopharm International SA (Industry)

Overall Status

Not yet recruiting

CT.gov ID

NCT05815160

Collaborator

(none)

Enrollment

Locations

Arms

Anticipated Duration (Months)

13.5

Patients Per Site

0.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The primary purpose of part 1 (dose escalation) of this study is to identify the recommended phase 2 dose (RP2D) and to characterize the safety and tolerability of Debio 0123 in combination with carboplatin and etoposide.

The primary purpose of part 2 (dose expansion) of this study is to characterize the safety and tolerability of Debio 0123 at the RP2D when administered in combination with carboplatin and etoposide.

Condition or Disease	Intervention/Treatment	Phase
Small Cell Lung Cancer Recurrent	Drug: Debio 0123 Drug: Etoposide Drug: Carboplatin	Phase 1

Study Design

Study Type:

Interventional

Anticipated Enrollment :

54 participants

Allocation:

Non-Randomized

Intervention Model:

Sequential Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase 1 Dose-Escalation and Expansion Study to Assess Safety and Preliminary Antitumor Activity of Debio 0123 in Combination With Carboplatin and Etoposide in Adult Participants With Small Cell Lung Cancer That Recurred or Progressed After Previous Standard Platinum-Based Therapy

Anticipated Study Start Date :

Apr 1, 2023

Anticipated Primary Completion Date :

Jan 1, 2026

Anticipated Study Completion Date :

Apr 1, 2026

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Part 1: Dose Escalation: Debio 0123 + Etoposide + Carboplatin Participants will receive Debio 0123 escalating doses, orally along with etoposide IV infusion and carboplatin IV infusion in 21-day cycles until disease progression or death or end of study.	Drug: Debio 0123 Administered as capsules. Drug: Etoposide Administered as IV infusion. Drug: Carboplatin Administered as IV infusion.
Experimental: Part 2: Dose Expansion: Debio 0123 + Etoposide + Carboplatin Participants will receive Debio 0123 RP2D determined in Part 1 of the study, orally along with etoposide IV infusion and carboplatin IV infusion in 21-day cycles until disease progression or death or end of study.	Drug: Debio 0123 Administered as capsules. Drug: Etoposide Administered as IV infusion. Drug: Carboplatin Administered as IV infusion.

Arm

Intervention/Treatment

Experimental: Part 1: Dose Escalation: Debio 0123 + Etoposide + Carboplatin

Participants will receive Debio 0123 escalating doses, orally along with etoposide IV infusion and carboplatin IV infusion in 21-day cycles until disease progression or death or end of study.

Drug: Debio 0123

Administered as capsules.

Drug: Etoposide

Administered as IV infusion.

Drug: Carboplatin

Administered as IV infusion.

Experimental: Part 2: Dose Expansion: Debio 0123 + Etoposide + Carboplatin

Participants will receive Debio 0123 RP2D determined in Part 1 of the study, orally along with etoposide IV infusion and carboplatin IV infusion in 21-day cycles until disease progression or death or end of study.

Drug: Debio 0123

Administered as capsules.

Drug: Etoposide

Administered as IV infusion.

Drug: Carboplatin

Administered as IV infusion.

Outcome Measures

Primary Outcome Measures

Part 1: Number of Participants Experiencing Dose-limiting Toxicities (DLTs) [Cycle 1 (Cycle=21 days)]
Parts 1 and 2: Number of Participants With at Least One Treatment Emergent Adverse Event (TEAE) [Approximately up to 44 months]
Parts 1 and 2: Number of Participants With Clinically Significant Abnormalities in Laboratory, Vital Signs, Electrocardiogram (ECG), and Echocardiogram Parameters [Approximately up to 44 months]
Parts 1 and 2: Change From Baseline in Eastern Cooperative Oncology Group Performance Status (ECOG PS) [Baseline up to approximately 44 months]

Secondary Outcome Measures

Parts 1 and 2: Trough Concentration (Ctrough) of Debio 0123 and its Metabolite [For Part 1: Predose from Day 2 to Day 11 of Cycle 1; For Part 2: Predose from Day 3 to Day 10 of Cycle 1 and only Day 8 of subsequent cycles (Cycle=21 days)]
Parts 1 and 2: Maximum Plasma Concentration (Cmax) of Debio 0123 and its Metabolite [For Part 1: Multiple timepoints post dose from Day 1 to Day 11 of Cycle 1 (Cycle=21 days); For Part 2: Will be derived from the population Pharmacokinetic (PK) model using the sparse samples collected]
Parts 1 and 2: Area Under the Concentration Curve Over 24 hours (AUC24h) of Debio 0123 and its Metabolite [For Part 1: Multiple timepoints post dose from Day 1 to Day 11 of Cycle 1 (Cycle=21 days); For Part 2: Will be derived from the population PK model using the sparse samples collected]
Part 1: Time to Maximum Plasma Concentration (tmax) of Debio 0123 and its Metabolite [Multiple timepoints post dose from Day 1 to Day 11 of Cycle 1 (Cycle=21 days)]
Part 1: Area Under the Concentration Curve up to the Last Measurable Concentration (AUClast) of Debio 0123 and its Metabolite [Multiple timepoints post dose from Day 1 to Day 21 of Cycle 1 and Day 1 of Cycle 2 (Cycle=21 days)]
Part 1: Area Under the Concentration Curve up to Infinity (AUCinf) of Debio 0123 and its Metabolite [Multiple timepoints post dose from Day 1 to Day 21 of Cycle 1 and Day 1 of Cycle 2 (Cycle=21 days)]
Part 1: Apparent Terminal Half-life (t1/2) of Debio 0123 and its Metabolite [Multiple timepoints post dose from Day 1 to Day 21 of Cycle 1 and Day 1 of Cycle 2 (Cycle=21 days)]
Part 1: Apparent Clearance (CL/F) of Debio 0123 [Multiple timepoints post dose from Day 1 to Day 21 of Cycle 1 and Day 1 of Cycle 2 (Cycle=21 days)]
Part 1: Apparent Volume of Distribution (Vd/F) of Debio 0123 [Multiple timepoints post dose from Day 1 to Day 21 of Cycle 1 and Day 1 of Cycle 2 (Cycle=21 days)]
Part 1: Maximum Plasma Concentration (Cmax) of Etoposide [Multiple timepoints from administration to post dose from Day 1 to Day 3 of Cycle 1 (Cycle=21 days)]]
Part 1: Area Under the Concentration Curve Over 24 hours (AUC24h) of Etoposide [Multiple timepoints post dose from Day 1 to Day 5 of Cycle 1 (Cycle=21 days)]
Part 1: Trough Concentration (Ctrough) of Etoposide [Predose from Day 2 to Day 5 of Cycle 1 (Cycle=21 days)]
Part 1: Maximum Plasma Concentration (Cmax) of Carboplatin [Multiple timepoints from administration up to 6 hours post dose on Day 1 of Cycle 1 (Cycle=21 days)]
Parts 1 and 2: Percentage of Participants With Best Overall Response (BOR) Assessed as per Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 Criteria [From the start of study treatment until disease progression or end of study (up to approximately 44 months)]
Parts 1 and 2: Percentage of Participants With Objective Response (OR) Assessed as per RECIST 1.1 Criteria [Up to end of study (approximately 44 months)]
Parts 1 and 2: Percentage of Participants With Disease Control (DC) Assessed as per RECIST 1.1 Criteria [From the start of study treatment until disease progression or end of study (up to approximately 44 months)]
Parts 1 and 2: Duration of Response (DOR) Assessed as per RECIST 1.1 Criteria [Up to disease progression or end of study (approximately 44 months)]
Parts 1 and 2: Progression Free Survival (PFS) Assessed as per RECIST 1.1 Criteria [From the start of study treatment until disease progression or death or end of study (up to approximately 44 months)]
Part 2: Overall Survival [From the start of study treatment until death from any cause or end of study (up to approximately 44 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically or cytologically confirmed SCLC
Tumor that is not bleeding
Prior platinum-based chemotherapy (carboplatin and/or cisplatin)

Part 1 (dose escalation): Recurrence or progression after a minimum of 45 days since the last dose of prior standard platinum-based therapy
Part 2 (expansion): Recurrence or progression after a minimum of 90 days since the last dose of prior standard platinum-based therapy

Measurable disease per RECIST 1.1
Willingness and ability to undergo tumor biopsy unless an archived tumor sample is available
ECOG performance status of 0-1
Life expectancy of at least 3 months in the best judgment of the Investigator
Adequate bone marrow, hepatic and renal function, adequate coagulation status
Willingness and ability to comply with scheduled visits, study treatment plans, laboratory tests, and other study procedures.

Exclusion Criteria:

Use of an investigational agent or medical device within 28 days prior to first dose of study treatment.
History of other malignancies requiring active treatment in the last 2 years prior to first dose of study treatment, except for superficial bladder cancers, ductal carcinoma in situ or other carcinomas in situ, and non-melanoma skin cancers (basal cell/squamous cell skin cancer) that have been treated with curative intent.
History of myocardial infarction or stroke in the last 6 months prior to first dose of study treatment, congestive heart failure greater than New York Heart Association (NYHA) class II, unstable angina pectoris, unexplained recurrent syncope, cardiac arrhythmia requiring treatment, known family history of sudden death from cardiac-related causes before the age of 50, or any cardiotoxicity experienced after previous chemotherapy.
Left ventricular ejection fraction (LVEF) below 55%.
QTcF >450 ms, history of congenital long QT syndrome, or clinically significant conduction abnormality, or any conduction abnormality that may increase the risk of TdP.
Clinically significant gastrointestinal abnormality that could affect the absorption of orally administered drugs
Major surgery ≤4 weeks prior to first dose of study treatment or incomplete recovery from the surgical procedure at the time of the first dose of study treatment.
Radiographic findings showing tumor involvement with large blood vessels or poor demarcation from them with increased risk for bleeding.
Radiographic findings of Interstitial lung disease (ILD) that are considered clinically significant.
Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage.
Any infection requiring the systemic use of an antibiotic or antiviral agent.
Known Hepatitis C virus (HCV), Hepatitis B virus (HBV), or Human Immunodeficiency Virus (HIV) infection. Participants with past infections that have been cured may be enrolled.
Immunization with live or live-attenuated vaccine within 28 days prior to first dose of study treatment.
Inability or unwillingness to swallow oral medications.
Chemotherapy, monoclonal antibodies/biologics, or radiotherapy with curative intent within 28 days prior to first dose of study treatment. Palliative radiation is allowed up to 1 week prior to study treatment start.
Unresolved AEs or toxicities due to previous treatments >Grade 1. Note: Participants with ≤Grade 2 alopecia or endocrinopathies controlled by replacement therapy are exceptions and may qualify for the study.
Hypersensitivity to Debio 0123, etoposide or carboplatin, or any of the excipients found in the formulations for Debio 0123, etoposide, or carboplatin. If a prior hypersensitivity to carboplatin has been observed but a successful desensitization was performed for the participant, he or she may be eligible for the study.
Prior exposure to any WEE1 inhibitor

Note: Other inclusion/exclusion criteria mentioned in the protocol may apply.

Contacts and Locations

Locations

	Site	City	Country	Postal Code
1	Clinica Universidad de Navarra	Madrid	Spain	28027
2	Hospital Universitario 12 de Octubre	Madrid	Spain	28041
3	Clinica Universidad de Navarra	Pamplona	Spain	31008
4	Hospital Clinico Universitario de Valencia	Valencia	Spain	46010