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

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)

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).

Study Overview

• Status: Completed
• Conditions: Refractory Chronic Cough
• Intervention / Treatment: Drug: 3 mg NOC-100 (via nebulizer); Drug: 1 mg NOC-110 (via DPI) [1x 1 mg capsule]; Drug: 3 mg NOC-110 (via DPI); Drug: Placebo (via DPI); Drug: 6 mg NOC-110 (via DPI); Drug: Placebo (via DPI) [2x Placebo capsules]

Detailed 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.

• Study Type: Interventional
• Enrollment (Actual): 24
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Arizona
    • Phoenix, Arizona, United States, 85283
      • Celerion
  • Florida
    • Leesburg, Florida, United States, 32789
      • Clinical Site Partners
    • Winter Park, Florida, United States, 34748
      • Clinical Site Partners

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Sequential Assignment
• Masking: Double

Number of Arms

8

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Part 1-Period 1-Treatment A; 3 mg NOC-100 (via nebulizer)	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
Placebo Comparator: Part 1-Periods 2 through 4 -Treatment B; 1 mg NOC-110 DPI (1 capsule)	Drug: 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
Placebo Comparator: Part 1-Periods 2 through 4 - Treatment C; 3mg NOC-110 DPI (1 capsule)	Drug: 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 Comparator: Part 1-Periods 2 through 4- Placebo; Placebo (1 capsule)	Drug: 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
Placebo Comparator: Part 1-Period 5- Treatment D; 6mg NOC-110 DPI (2 capsules)	Drug: 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 Comparator: Part 1-Period 5- Placebo; Placebo (2 capsules)	Drug: 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
Placebo Comparator: Part 2- Active; 6mg NOC-110 DPI (2 capsules)	Drug: 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 Comparator: Part 2- Placebo; Placebo DPI (2 capsules)	Drug: 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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
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 Outcome Measures

Outcome Measure	Measure Description	Time Frame
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

Collaborators and Investigators

• Sponsor: Nocion Therapeutics
• Investigators: Study Director: Christopher Silber, MD, Nocion Therapeutics, Inc.

Study record dates

Study Major Dates

• Study Start (Actual): February 7, 2022
• Primary Completion (Actual): October 25, 2022
• Study Completion (Actual): October 25, 2022

Study Registration Dates

• First Submitted: November 2, 2022
• First Submitted That Met QC Criteria: November 16, 2022
• First Posted (Actual): November 29, 2022

Study Record Updates

• Last Update Posted (Actual): March 30, 2023
• Last Update Submitted That Met QC Criteria: March 29, 2023
• Last Verified: November 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Respiration Disorders; Signs and Symptoms, Respiratory; Cough
• Other Study ID Numbers: NOC110-C-102

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No