Placebo-controlled, Single and Multiple Dose Study in Healthy Volunteers and Refractory Chronic Cough Patients to Assess the Safety, Tolerability, and Pharmacokinetics of Two Formulations of NTX-1175

Refractory Chronic Cough Clinical Trial

Official title:

A Phase 1, Two Part, Placebo-controlled, Single Dose Study in Healthy Volunteers and Multiple Dose Study in Patients With Refractory Chronic Cough to Assess the Safety, Tolerability, and PK of NTX-1175 Administered Via Nebulizer (NOC-100) and Dry Powder Inhaler (NOC-110)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05628740
• Other study ID #: NOC110-C-102
• Status: Completed
• Phase: Phase 1
• Start date: February 7, 2022
• Est. completion date: October 25, 2022

Study information

• Verified date: November 2022
• Source: Nocion Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Part 1 will evaluate the safety, tolerability and PK of single doses of three dose levels of NTX-1175 drug substance administered by dry powder inhaler (NOC-110) compared to a single dose reference nebulizer (NOC-100) treatment in healthy participants. Part 2 will evaluate the safety, tolerability and PK of multiple doses of NTX-1175 drug substance administered by dry powder inhaler (NOC-110) to participants with refractory chronic cough. Part 2 will also evaluate the treatment effect of multiple doses of one dose level of NTX-1175 drug substance administered by dry powder inhaler (NOC-110).

Description:

Part 1 is a randomized, double-blinded 3 period crossover and 1 period parallel study of single dose administration of NOC-110 via dry powder inhaler, preceded by a reference period of NOC-100 administered via nebulizer. A total of 12 healthy participants will be enrolled to ensure that 9 participants complete this part of study. Part 2 is a randomized, double-blinded, placebo-controlled, multiple-dose, parallel design study in patients with refractory chronic cough. A total of 12 participants will be enrolled to ensure that 8 participants complete this part of study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: October 25, 2022
• Est. primary completion date: October 25, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

Participants must meet all of the following criteria to be eligible for participation in

the study:

1. Male or female participants between the ages of 18 to 65 years, inclusive, at the time of screening (Part 1) and between the ages of 18 to 85 years, inclusive, at the time of screening (Part 2).

2. Has had rCC diagnosis for = 12 months (Part 2) prior to screening.

3. Awake-cough frequency of =20 per hour (average) at Screening (Part 2).

4. Score of =40 mm on the Cough Severity Visual Analog Scale (VAS) at Screening (Part 2).

5. Chest radiograph or CT thorax within the last 60 months not demonstrating any abnormality considered to be significantly contributing to the rCC. (Part 2)

6. Body mass index (BMI) =19.0 and =32.0 kg/m2, inclusive, at Screening.

7. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) <2 x upper limit of normal (ULN); alkaline phosphatase (ALP) and bilirubin =1.5 x ULN (isolated bilirubin >1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).

8. Creatinine clearance =50 mL/min.

9. Must be fully SARS-CoV-2 vaccinated.

10. Must be SARS-CoV-2 negative via rapid antigen testing or polymerase chain reaction (PCR) test at Screening and PCR at Check-in Day -1.

11. In the Investigator's opinion, has no clinically significant disease and/or clinically significant abnormal laboratory values as determined by the Investigator based on medical history, physical examination, or laboratory evaluations conducted at the screening visit or on admission to the clinical research unit. Exclusion Criteria: Participants who meet any one of the following criteria will be deemed ineligible for

participation in the study:

1. Is found to have positive test for SARS-CoV-2 at Screening or Check-in Day -1, whether or not this was accompanied by the clinical symptoms of COVID-19.

2. Current smoker or individuals who have given up smoking within the past 6 months prior to screening, or those with >20 pack-year smoking history (Part 2)

3. Current diagnosis of chronic obstructive pulmonary disease (COPD), bronchiectasis, unexplained pulmonary fibrosis, or asthma (Part 2).

4. History or presence of alcohol or drug use disorder, per Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5), within the past 2 years prior to screening.

5. Current opiate/opioid use in the past 7 days prior to screening, or medical history of opiate/opioid use disorder.

6. Unable to refrain from the use of:

1. Gabapentin, pregabalin, and/or amitryptline or other tricyclics within 4 weeks prior to screening and throughout the study (Part 2)

2. Chronic, systemic corticosteroid use within 4 weeks prior to screening and throughout the study (Part 2).

3. Inhalers including long-acting and short acting beta 2-agonists (LABA and SABA), and inhaled corticosteroids (ICS) within 8 weeks prior to screening and throughout the study.

4. Lidocaine or related compounds of any form within 14 days prior to screening and throughout the study (Part 2).

5. Medication or remedies to aid sleeping 14 days prior to screening and throughout the study (Part 2).

6. Angiotensin-converting enzyme (ACE)-inhibitor within 12 weeks prior to screening and throughout the study (Part 2).

7. Antitussives 7 days prior to screening and throughout the study (Part 2).

8. Speech and language therapy for rCC within 4 weeks prior to screening and throughout the study (Part 2).

9. Food and beverages containing alcohol for 24 hours prior to screening (Part 2).

7. History or presence of cardiac dysfunction including arrhythmia, bundle branch block; Wolff Parkinson White syndrome, recent thromboembolic event, prolonged PR (=220 msec), QRS (=120 msec), QTcF interval (=450 msec [males] or =470 msec [females]) or has ECG findings deemed abnormal with clinical significance by the Investigator or designee at Screening.

8. Positive results at Screening for HIV, HBsAg, or HCV (participants successfully treated for HCV may be permitted at the discretion of the Investigator).

9. Supine blood pressure is less than 90/40 mmHg or greater than 140/90 mmHg (Part 1), or greater than 160/95 mmHg (Part 2) at Screening. Vital signs may be repeated twice.

10. Supine heart rate is lower than 40 beats per minute (bpm) or higher than 99 bpm at Screening. Vital signs may be repeated twice.

11. History of asthma or COPD (Part 1).

12. Forced expiratory volume in 1 second/ forced vital capacity (FEV1/FVC) < lower limit of normal (LLN) per Global Lung Health Initiative normative dataset at Screening.

13. Had symptoms of any significant acute illness, including symptoms of COVID-19 within 30 days before the start of the study (time of first dose), as determined by the Investigator.

Related Conditions & MeSH terms

• Cough
• Refractory Chronic Cough

Intervention

Drug:
• 3 mg NOC-100 (via nebulizer)
Participants determined to be eligible for Part 1 of the study will be enrolled and will be assigned to receive a single dose of the reference nebulizer treatment of NOC 100 at 3 mg (Treatment A) in Period 1
• 1 mg NOC-110 (via DPI) [1x 1 mg capsule]
Participants will be randomized to receive single doses of 1 mg NOC-110 (via DPI) in a crossover fashion according to a prespecified randomization schedule
• 3 mg NOC-110 (via DPI)
Participants will be randomized to receive single doses of 3 mg NOC-110 (via DPI) in a crossover fashion according to a prespecified randomization schedule
• Placebo (via DPI)
Participants will be randomized to receive single doses of placebo via capsule in a crossover fashion according to a prespecified randomization schedule
• 6 mg NOC-110 (via DPI)
Participants will be randomized to receive single doses of 6 mg NOC-110 via DPI in a parallel fashion according to a prespecified randomization schedule
• Placebo (via DPI) [2x Placebo capsules]
Participants will be randomized to receive single doses of Placebo (via DPI) [2x Placebo capsules] in a parallel fashion according to a prespecified randomization schedule

Locations

Country	Name	City	State
United States	Clinical Site Partners	Leesburg	Florida
United States	Celerion	Phoenix	Arizona
United States	Clinical Site Partners	Winter Park	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Nocion Therapeutics

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number and severity of Treatment Emergent Adverse Events (TEAEs) following single doses of NOC-110 or placebo administered with a DPI	To evaluate the safety and tolerability of single doses of three dose levels of NTX-1175 drug substance administered by DPI (Drug Product NOC-110) compared to a single dose reference nebulizer treatment (Drug Product NOC-100) in healthy participants, number and severity of TEAEs following single doses of NOC-110 or placebo administered with a DPI compared to a reference period administration of NOC 100 via a nebulizer in healthy adult participants will be reported.	Part 1- Screening through Day 23
Primary	Number and severity of TEAE following repeat doses of NOC 110 compared to placebo in participants with chronic cough.	To evaluate the safety and tolerability of multiple doses of NOC-110 administered by DPI to participants with refractory chronic cough (rCC), number and severity of TEAE following repeat doses of NOC 110 compared to placebo in participants with chronic cough will be reported.	Part 2- Screening through Day 12
Secondary	Peak plasma concentration (Cmax) of single doses of three dose levels of NOC-110 administered by DPI compared to a single dose reference nebulizer treatment (NOC-100) in healthy participants.	PK parameters for plasma NTX-1175: Cmax	Part 1- Day 1, Day 5, Day 9, Day 13 and Day 17
Secondary	The time to reach maximum observed concentration (Tmax) of single doses of three dose levels of NOC-110 administered by DPI compared to a single dose reference nebulizer treatment (NOC-100) in healthy participants.	PK parameters for plasma NTX-1175: Tmax	Part 1- Day 1, Day 5, Day 9, Day 13 and Day 17
Secondary	The area under the concentration-time (AUC) curve of single doses of three dose levels of NOC-110 compared to a single dose reference nebulizer treatment in healthy participants.	PK parameters for plasma NTX-1175: AUC [time 0 to the last observed non-zero concentration (t) (AUC0-t), time 0 to Hour 24 (AUC0-24), time 0 extrapolated to infinity (AUC0-inf), percent of AUC0 inf extrapolated (AUC%extrap)]	Part 1- Day 1, Day 5, Day 9, Day 13 and Day 17
Secondary	The time of the last measurable concentration (Tlast) of single doses of three dose levels of NOC-110 administered by DPI compared to a single dose reference nebulizer treatment (NOC-100) in healthy participants.	PK parameters for plasma NTX-1175: Tlast	Part 1- Day 1, Day 5, Day 9, Day 13 and Day 17
Secondary	The apparent terminal elimination half-life (t½) of single doses of three dose levels of NOC-110 administered by DPI compared to a single dose reference nebulizer treatment (NOC-100) in healthy participants.	PK parameters for plasma NTX-1175: t½	Part 1- Day 1, Day 5, Day 9, Day 13 and Day 17
Secondary	The apparent terminal elimination rate constant (Kel) of single doses of three dose levels of NOC-110 administered by DPI compared to a single dose reference nebulizer treatment (NOC-100) in healthy participants.	PK parameters for plasma NTX-1175: Kel	Part 1- Day 1, Day 5, Day 9, Day 13 and Day 17
Secondary	The Cmax of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Cmax and maximum observed concentration at steady-state (Cmax, ss)	Part 2- Day 1, Day 5
Secondary	The Tmax of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Tmax, time to reach Cmax,ss (Tmax,ss)	Part 2- Day 1, Day 5
Secondary	The AUC of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: AUC0-t AUC0-inf AUC%extrap	Part 2- Day 1, Day 5
Secondary	The Tlast of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Tlast	Part 2- Day 1, Day 5
Secondary	The t½ of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: t½	Part 2- Day 1, Day 5
Secondary	The Kel multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Kel	Part 2- Day 1, Day 5
Secondary	The concentration observed at the end of the dosing interval (Ctrough) of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Ctrough	Part 2- Days 2 to 4
Secondary	The minimum observed non zero concentration between dose time and dose time + dosing interval (tau) (min,ss,) of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Cmin,ss	Part 2- Day 5
Secondary	The area under the concentration-time curve during a dosing interval (tau), at steady state (AUCtau) of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: AUCtau	Part 2- Day 5
Secondary	The average concentration during a dosing interval, at steady state (Cavg,ss) of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: Cavg,ss	Part 2- Day 5
Secondary	The accumulation (R) of multiple doses of NOC 110 administered by DPI to participants with rCC.	PK parameters for plasma NTX-1175: R	Part 2- Day 5
Secondary	Awake-coughs per hour in participants with rCC	The treatment effect of multiple doses of one dose level of NOC-110 administered by DPI, as determined by awake-coughs per hour in participants with rCC.	Part 2- Screening, Day -1, Day 1, Day 3 and Day 5