Study to Evaluate the Effect of Bosentan on the Pharmacokinetics of Lurbinectedin in Patients With Advanced Solid Tumors

Advanced Solid Tumor Clinical Trial

Official title:

An Open-Label, Multicenter Study to Assess the Potential Effects of Bosentan (a Moderate CYP3A4 Inducer) on the Pharmacokinetics of Lurbinectedin (PM01183) in Patients With Advanced Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05072106
• Other study ID #: PM1183-A-019-20
• Status: Recruiting
• Phase: Phase 1
• Start date: January 14, 2021
• Est. completion date: November 1, 2022

Study information

• Verified date: September 2021
• Source: PharmaMar
• Contact: Pharma Mar, S.A.
• Phone: +3491 846 6077
• Email: cmfernandez[@]pharmamar.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Prospective, open-label, two-way crossover, phase Ib drug-drug interaction study in patients with advanced solid tumors. The study consisting of two lurbinectedin cycles, one cycle in combination with bosentan and one cycle as single agent (in different order depending on the study sequence), and one additional third cycle of lurbinectedin as a single agent for patients who meet the continuation criteria and obtain a clinical benefit after the first two cycles.

Description:

All patients will receive a maximum of three cycles: two consecutive cycles of lurbinectedin, one cycle with and one cycle without bosentan co-administration (in different order depending on the study Sequence 1 or Sequence 2 of treatment), followed by a third cycle with lurbinectedin alone (this last optional for patients with clinical benefit). Lurbinectedin will be administered as a 1-hour intravenous (i.v.) infusion every three weeks (q3wk) via a central or peripheral vein. The dose of lurbinectedin will be 3.2 mg/m² for all patients when administered with and without bosentan. If toxicity occurs, the appropriate intra-patient dose level (DL) reductions will be implemented in the subsequent cycle. Patients will be randomized in a 1:1 ratio to Sequence 1 (TR: Test-Reference; lurbinectedin + bosentan in Cycle 1) or Sequence 2 (RT: reference-Test; lurbinectedin + bosentan in Cycle 2). Patients will receive lurbinectedin until disease progression, unacceptable toxicity, consent withdrawal or while it is considered to be in their best interest. Treatment with lurbinectedin outside this study could be continued under a Compassionate Use Agreement after the completion of the optional third study cycle.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 8
• Est. completion date: November 1, 2022
• Est. primary completion date: October 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Voluntary signed and dated written informed consent prior to any specific study procedure.

2. Male or female with age = 18 years.

3. Eastern Cooperative Oncology Group (ECOG) performance status (PS) = 1.

4. Life expectancy > 3 months.

5. Pathologically confirmed diagnosis of advanced solid tumors [except for primary central nervous system (CNS) tumors], for which no approved therapy exists.

6. Recovery to grade = 1 from drug-related adverse events (AEs) of previous treatments, excluding alopecia and grade =2 asthenia or fatigue, according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE v.5).

7. Laboratory values within fourteen days prior to registration: a) Absolute neutrophil count (ANC) > 2.0 x 109/L, platelet count > 120 x 109/L and hemoglobin > 9.0 g/dL (patients may be transfused as clinically indicated prior to study entry). b) Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) = 2.5 x upper limit of normal (ULN). c) Serum total bilirubin = 1.0 x ULN. If total bilirubin is > 1.0 x ULN, but = 1.5 x ULN, direct bilirubin must be = 1.0 x ULN. d) Albumin = 3.5 g/dL. e) Creatinine clearance (CLcr) >= 30 mL/min (using Cockcroft and Gault's formula). f) Creatine phosphokinase (CPK) = 2.5 x ULN.

8. Left ventricular ejection fraction (LVEF) by echocardiography (ECHO) or multiple-gated acquisition (MUGA) within normal range (according to institutional standards).

9. Evidence of non-childbearing status for women of childbearing potential (WOCBP). WOCBP must agree to use a highly effective contraceptive measure up to six months after treatment discontinuation. As bosentan may render hormonal contraceptives ineffective, and taking into account the teratogenic effects observed in animals, hormonal contraceptives cannot be the sole method of contraception during treatment with bosentan. Fertile male patients with WOCBP partners should use condoms during treatment and for four months following the last investigational medicinal product (IMP) dose.

Exclusion Criteria:

1. Concomitant diseases/conditions: a) History or presence of unstable angina, myocardial infarction, congestive heart failure, or clinically significant valvular disease within last year. b) Symptomatic arrhythmia or any uncontrolled arrhythmia requiring ongoing treatment. c) Known cirrhosis, alcohol induced steatosis, or chronic active hepatitis. For hepatitis B, this includes positive test for both Hepatitis B surface antigen (HBsAg) and quantitative Hepatitis B polymerase chain reaction (PCR or HVB-DNA+). For hepatitis C, this includes positive test for both Hepatitis C antibody and quantitative Hepatitis C by PCR (or HVCRNA+). d) History of obstructive cholestatic liver disease (suitable for stenting procedure) or biliary sepsis in the past 2 months. e) Active COVID-19 disease (this includes positive test for SARS-CoV-2 in nasopharyngeal/oropharyngeal swabs or nasal swabs by PCR).

2. Symptomatic, progressive or corticosteroids-requiring documented brain metastases or leptomeningeal disease involvement. Patients with asymptomatic documented stable brain metastases not requiring corticosteroids during the last four weeks are allowed.

3. Use of (strong or moderate) inhibitors or inducers of CYP3A4 activity within three weeks prior to Day 1 of Cycle 1.

4. Use of CYP3A4 substrates for which concomitant administration with moderate CYP3A4 inductor is contraindicated.

5. Treatment with any investigational product within the 30 days before Day 1 of Cycle 1.

6. Women who are pregnant or breast-feeding and fertile patients (men and women) who are not using an effective method of contraception.

7. Psychiatric illness/social situations that would limit compliance with study requirements.

Related Conditions & MeSH terms

• Advanced Solid Tumor
• Neoplasms

Intervention

Drug:
• Lurbinectedin
3.2 mg/m² as a 1-hour i.v. infusion on Day 1.
• Bosentan
Bosentan: 125 mg (one film-coated tablet of 125 mg) orally (p.o.) twice daily in the morning and in the evening during the prior five consecutive days before the day of lurbinectedin infusion (Day 1), and once daily on Day 1 (before lurbinectedin infusion).

Locations

Country	Name	City	State
Spain	Fundación Jiménez Diaz	Madrid
Spain	Hospital de Sanchinarro	Madrid

Sponsors (1)

Lead Sponsor	Collaborator
PharmaMar

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose-normalized maximum observed plasma concentration (Cmax) of total lurbinectedin: Alone and in combination with bosentan.	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Primary	Dose-normalized area under the plasma concentration-time profile from time zero to extrapolated infinity (AUC0-8) of total Lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized area under the plasma concentration-time profile from time zero to last quantifiable concentration (AUC0-t) of total lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Plasma clearance (CL) of total lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Plasma volume of distribution at steady-state (Vss) of total lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Terminal elimination half-life (t1/2) in plasma of total lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized maximum observed plasma concentration (Cu,max) of unbound lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized area under the plasma concentration-time profile from time zero to extrapolated infinity (AUCu,0-8) of unbound Lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Plasma clearance (CLu) of unbound lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Plasma volume of distribution at steady-state (Vss,u) of unbound lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Terminal elimination half-life (t1/2,u) in plasma of unbound lurbinectedin: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7, 25, 49, 97 and 169 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized maximum observed plasma concentration (Cmax) of total lurbinectedin metabolite M1: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7 and 25 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized area under the plasma concentration-time profile from time zero to extrapolated infinity (AUC0-8) of total lurbinectedin metabolite M1: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7 and 25 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized area under the plasma concentration-time profile from time zero to last quantifiable concentration (AUC0-t) of total lurbinectedin metabolite M1: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7 and 25 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized maximum observed plasma concentration (Cmax) of total lurbinectedin metabolite M4: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7 and 25 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized area under the plasma concentration-time profile from time zero to extrapolated infinity (AUC0-8) of total lurbinectedin metabolite M4: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7 and 25 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Dose-normalized area under the plasma concentration-time profile from time zero to last quantifiable concentration (AUC0-t) of total lurbinectedin metabolite M4: Alone and in combination with bosentan	Pharmacokinetic analyses will be evaluated in plasma by standard non-compartmental methods, or population methods, if necessary.	Preinfusion, 0.917, 1.5, 2, 3, 5, 7 and 25 hours post lurbinectedin infusion start on Day 1 of Cycle 1 or Cycle 2 (each cycle is 21 days)
Secondary	Number of patients with Treatment Emergent Adverse Events (AEs)	Graded according to the NCI-CTCAE v.5.	Baseline up to end of study (up to 83 days)
Secondary	Number of patients with Serious Adverse Events (SAEs)	Graded according to the NCI-CTCAE v.5.	Baseline up to end of study (up to 83 days)
Secondary	Number of patients with Abnormalities in Laboratory Parameters	Graded according to the NCI-CTCAE v.5.	Baseline up to end of study (up to 83 days)
Secondary	The presence or absence of germinal genetic polymorphisms in genes relevant for lurbinectedin disposition	Lurbinectedin disposition (distribution, metabolism and excretion) from a single blood sample	Day 1 of Cycle 1 (each cycle is 21 days)