Clinical Trials Register

Summary
EudraCT Number:	2018-004447-23
Sponsor's Protocol Code Number:	RVT1601-CC-04
National Competent Authority:	Czechia - SUKL
Clinical Trial Type:	EEA CTA
Trial Status:	Completed
Date on which this record was first entered in the EudraCT database:	2019-03-14
Trial results	View results

Index
A. PROTOCOL INFORMATION
B. SPONSOR INFORMATION
C. APPLICANT IDENTIFICATION
D. IMP IDENTIFICATION
D.8 INFORMATION ON PLACEBO
E. GENERAL INFORMATION ON THE TRIAL
F. POPULATION OF TRIAL SUBJECTS
G. INVESTIGATOR NETWORKS TO BE INVOLVED IN THE TRIAL
N. REVIEW BY THE COMPETENT AUTHORITY OR ETHICS COMMITTEE IN THE COUNTRY CONCERNED
P. END OF TRIAL

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A. Protocol Information

A.1

Member State Concerned

Czechia - SUKL

A.2

EudraCT number

2018-004447-23

A.3

Full title of the trial

Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging, Efficacy and Safety Study with Inhaled RVT-1601 for the Treatment of Persistent Cough in Patients with Idiopathic Pulmonary Fibrosis (IPF): SCENIC Trial

Randomizované, dvojitě zaslepené, placebem kontrolované klinické
hodnocení s různými rozsahy dávek, zkoumající účinnost a bezpečnost
inhalovaného přípravku RVT-1601 při léčbě přetrvávajícího kašle u
pacientů s idiopatickou plicní fibrózou (IPF): klinické hodnocení SCENIC

A.3.1

Title of the trial for lay people, in easily understood, i.e. non-technical, language

Efficacy and Safety Study with Inhaled RVT-1601 for the Treatment of Persistent Cough in Patients with Idiopathic Pulmonary Fibrosis (IPF)

A.3.2

Name or abbreviated title of the trial where available

SCENIC Trial

A.4.1

Sponsor's protocol code number

RVT1601-CC-04

A.7

Trial is part of a Paediatric Investigation Plan

A.8

EMA Decision number of Paediatric Investigation Plan

B. Sponsor Information
B.Sponsor: 1
B.1.1	Name of Sponsor	Respivant Sciences GmbH
B.1.3.4	Country	Switzerland
B.3.1 and B.3.2	Status of the sponsor	Commercial
B.4 Source(s) of Monetary or Material Support for the clinical trial:
B.4.1	Name of organisation providing support	Respivant Sciences GmbH
B.4.2	Country	Switzerland
B.5 Contact point designated by the sponsor for further information on the trial
B.5.1	Name of organisation	Respivant Sciences, Inc.
B.5.2	Functional name of contact point	Ahmet Tutuncu
B.5.3	Address:
B.5.3.1	Street Address	11455 El Camino Real, Suite 460
B.5.3.2	Town/ city	San Diego, California
B.5.3.3	Post code	92130
B.5.3.4	Country	United States
B.5.4	Telephone number	+1 (858) 436-1600
B.5.6	E-mail	atutuncu@respivant.com

D. IMP Identification
D.IMP: 1
D.1.2 and D.1.3	IMP Role	Test
D.2	Status of the IMP to be used in the clinical trial
D.2.1	IMP to be used in the trial has a marketing authorisation	No
D.2.5	The IMP has been designated in this indication as an orphan drug in the Community	No
D.2.5.1	Orphan drug designation number
D.3 Description of the IMP
D.3.1	Product name	Cromolyn sodium [Disodium Cromoglycate]
D.3.2	Product code	RVT-1601 (formerly, PA101B)
D.3.4	Pharmaceutical form	Nebulisation solution
D.3.4.1	Specific paediatric formulation	No
D.3.7	Routes of administration for this IMP	Inhalation use
D.3.8 to D.3.10 IMP Identification Details (Active Substances)
D.3.8	INN - Proposed INN	SODIUM CROMOGLICATE
D.3.9.1	CAS number	15826-37-6
D.3.9.2	Current sponsor code	RVT-1601 (formerly, PA101B)
D.3.9.3	Other descriptive name	SODIUM CROMOGLICATE
D.3.9.4	EV Substance Code	SUB12286MIG
D.3.10	Strength
D.3.10.1	Concentration unit	mg/ml milligram(s)/millilitre
D.3.10.2	Concentration type	not less then
D.3.10.3	Concentration number	7.5
D.3.11 The IMP contains an:
D.3.11.1	Active substance of chemical origin	Yes
D.3.11.2	Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP)	No
	The IMP is a:
D.3.11.3	Advanced Therapy IMP (ATIMP)	No
D.3.11.3.1	Somatic cell therapy medicinal product	No
D.3.11.3.2	Gene therapy medical product	No
D.3.11.3.3	Tissue Engineered Product	No
D.3.11.3.4	Combination ATIMP (i.e. one involving a medical device)	No
D.3.11.3.5	Committee on Advanced therapies (CAT) has issued a classification for this product	No
D.3.11.4	Combination product that includes a device, but does not involve an Advanced Therapy	Yes
D.3.11.5	Radiopharmaceutical medicinal product	No
D.3.11.6	Immunological medicinal product (such as vaccine, allergen, immune serum)	No
D.3.11.7	Plasma derived medicinal product	No
D.3.11.8	Extractive medicinal product	No
D.3.11.9	Recombinant medicinal product	No
D.3.11.10	Medicinal product containing genetically modified organisms	No
D.3.11.11	Herbal medicinal product	No
D.3.11.12	Homeopathic medicinal product	No
D.3.11.13	Another type of medicinal product	No
D.IMP: 2
D.1.2 and D.1.3	IMP Role	Test
D.2	Status of the IMP to be used in the clinical trial
D.2.1	IMP to be used in the trial has a marketing authorisation	No
D.2.5	The IMP has been designated in this indication as an orphan drug in the Community	No
D.2.5.1	Orphan drug designation number
D.3 Description of the IMP
D.3.1	Product name	Cromolyn sodium [Disodium Cromoglycate]
D.3.2	Product code	RVT-1601 (formerly, PA101B)
D.3.4	Pharmaceutical form	Nebulisation solution
D.3.4.1	Specific paediatric formulation	No
D.3.7	Routes of administration for this IMP	Inhalation use
D.3.8 to D.3.10 IMP Identification Details (Active Substances)
D.3.8	INN - Proposed INN	SODIUM CROMOGLICATE
D.3.9.1	CAS number	15826-37-6
D.3.9.2	Current sponsor code	RVT-1601 (formerly, PA101B)
D.3.9.3	Other descriptive name	SODIUM CROMOGLICATE
D.3.9.4	EV Substance Code	SUB12286MIG
D.3.10	Strength
D.3.10.1	Concentration unit	mg/ml milligram(s)/millilitre
D.3.10.2	Concentration type	not less then
D.3.10.3	Concentration number	30
D.3.11 The IMP contains an:
D.3.11.1	Active substance of chemical origin	Yes
D.3.11.2	Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP)	No
	The IMP is a:
D.3.11.3	Advanced Therapy IMP (ATIMP)	No
D.3.11.3.1	Somatic cell therapy medicinal product	No
D.3.11.3.2	Gene therapy medical product	No
D.3.11.3.3	Tissue Engineered Product	No
D.3.11.3.4	Combination ATIMP (i.e. one involving a medical device)	No
D.3.11.3.5	Committee on Advanced therapies (CAT) has issued a classification for this product	No
D.3.11.4	Combination product that includes a device, but does not involve an Advanced Therapy	Yes
D.3.11.5	Radiopharmaceutical medicinal product	No
D.3.11.6	Immunological medicinal product (such as vaccine, allergen, immune serum)	No
D.3.11.7	Plasma derived medicinal product	No
D.3.11.8	Extractive medicinal product	No
D.3.11.9	Recombinant medicinal product	No
D.3.11.10	Medicinal product containing genetically modified organisms	No
D.3.11.11	Herbal medicinal product	No
D.3.11.12	Homeopathic medicinal product	No
D.3.11.13	Another type of medicinal product	No
D.IMP: 3
D.1.2 and D.1.3	IMP Role	Test
D.2	Status of the IMP to be used in the clinical trial
D.2.1	IMP to be used in the trial has a marketing authorisation	No
D.2.5	The IMP has been designated in this indication as an orphan drug in the Community	No
D.2.5.1	Orphan drug designation number
D.3 Description of the IMP
D.3.1	Product name	Cromolyn sodium [Disodium Cromoglycate]
D.3.2	Product code	RVT-1601 (formerly, PA101B)
D.3.4	Pharmaceutical form	Nebulisation solution
D.3.4.1	Specific paediatric formulation	No
D.3.7	Routes of administration for this IMP	Inhalation use
D.3.8 to D.3.10 IMP Identification Details (Active Substances)
D.3.8	INN - Proposed INN	SODIUM CROMOGLICATE
D.3.9.1	CAS number	15826-37-6
D.3.9.2	Current sponsor code	RVT-1601 (formerly, PA101B)
D.3.9.3	Other descriptive name	SODIUM CROMOGLICATE
D.3.9.4	EV Substance Code	SUB12286MIG
D.3.10	Strength
D.3.10.1	Concentration unit	mg/ml milligram(s)/millilitre
D.3.10.2	Concentration type	not less then
D.3.10.3	Concentration number	60
D.3.11 The IMP contains an:
D.3.11.1	Active substance of chemical origin	Yes
D.3.11.2	Active substance of biological/ biotechnological origin (other than Advanced Therapy IMP (ATIMP)	No
	The IMP is a:
D.3.11.3	Advanced Therapy IMP (ATIMP)	No
D.3.11.3.1	Somatic cell therapy medicinal product	No
D.3.11.3.2	Gene therapy medical product	No
D.3.11.3.3	Tissue Engineered Product	No
D.3.11.3.4	Combination ATIMP (i.e. one involving a medical device)	No
D.3.11.3.5	Committee on Advanced therapies (CAT) has issued a classification for this product	No
D.3.11.4	Combination product that includes a device, but does not involve an Advanced Therapy	Yes
D.3.11.5	Radiopharmaceutical medicinal product	No
D.3.11.6	Immunological medicinal product (such as vaccine, allergen, immune serum)	No
D.3.11.7	Plasma derived medicinal product	No
D.3.11.8	Extractive medicinal product	No
D.3.11.9	Recombinant medicinal product	No
D.3.11.10	Medicinal product containing genetically modified organisms	No
D.3.11.11	Herbal medicinal product	No
D.3.11.12	Homeopathic medicinal product	No
D.3.11.13	Another type of medicinal product	No

D.8 Information on Placebo
D.8 Placebo: 1
D.8.1	Is a Placebo used in this Trial?	Yes
D.8.3	Pharmaceutical form of the placebo	Nebulisation solution
D.8.4	Route of administration of the placebo	Inhalation use

E. General Information on the Trial

E.1 Medical condition or disease under investigation

E.1.1

Medical condition(s) being investigated

Persistent cough in Idiopathic Pulmonary Fibrosis (IPF)

E.1.1.1

Medical condition in easily understood language

Cough in IPF is often a debilitating symptom that adversely affects quality of life (QoL) and is usually refractory to medical therapy.

E.1.1.2

Therapeutic area

Diseases [C] - Respiratory Tract Diseases [C08]

MedDRA Classification

E.1.2 Medical condition or disease under investigation

E.1.2	Version	21.1
E.1.2	Level	LLT
E.1.2	Classification code	10070801
E.1.2	Term	Persistent cough
E.1.2	System Organ Class	100000004855

E.1.3

Condition being studied is a rare disease

Yes

E.2 Objective of the trial

E.2.1

Main objective of the trial

Primary:
• To assess the efficacy of inhaled RVT-1601 in comparison with placebo following 12 weeks of treatment

E.2.2

Secondary objectives of the trial

Secondary:
• To select the optimal dose of RVT-1601
• To assess the pharmacokinetic (PK) profile of RVT-1601
• To assess biomarker response to RVT-1601
• To assess the impact of RVT-1601 on IPF disease
• To assess the safety of RVT-1601

E.2.3

Trial contains a sub-study

Yes

E.2.3.1

Full title, date and version of each sub-study and their related objectives

PK analysis

E.3

Principal inclusion criteria

Inclusion criteria:
1. Male or female subjects age 40 through 89 years, inclusive
2. Confirmed diagnosis of IPF with clinical features consistent with the
current clinical practice guidelines for IPF
3. Presence of persistent cough for at least 8 weeks that is primarily due
to IPF and not responsive to antitussive therapy
4. Daytime cough severity score of ≥40 mm on a 100-mm VAS at the
Screening Visit
5. 24-hour average cough count of at least 10 coughs per hour using an
objective cough-count monitor during Screening
6. Forced Vital Capacity (FVC) ≥ 45% predicted value within 4 weeks of
the Screening Visit
7. Life expectancy of at least 12 months
8. Willing and able to follow the study required visits and assessments
9. Willing and able to use the cough monitor for 24-hour periods at
select study visits
10. Willing and able to provide written informed consent prior to study-related
procedures

E.4

Principal exclusion criteria

Exclusion criteria:
1. Current or recent history of clinically significant medical condition, laboratory abnormality, or illness that could place the subject at risk or compromise the quality of the study data as determined by the investigator
2. Significant coronary artery disease (i.e., myocardial infarction within 6 months or unstable angina within 1 month of the Screening Visit)
3. An upper or lower respiratory tract infection within 4 weeks of the Screening Visit
4. Acute exacerbation of IPF within 6 months of the Screening Visit (Collard et al., 2016)
5. Lung transplantation expected within 12 months
6. Requiring supplemental O2 ≥ 4 litres/min to maintain peripheral
arterial O2 saturation (SpO2) ≥ 88% at rest
7. History of malignancy likely to result in significant disability or likely
to require significant medical or surgical intervention within the next 2
years. This does not include minor surgical procedures for localized
cancer (e.g., basal cell carcinoma, squamous cell, prostate carcinoma or
cervical
carcinoma in situ)
8. Current smoker (i.e., use of tobacco products within the last 3
months)
9. Current or recent history of drug or alcohol abuse within 12 months of
the Screening Visit
10. Participation in any other investigational drug study within 4 weeks
of the Screening Visit or within 5 times the elimination half- life of an
investigational drug
11. Use of the following drugs for cough management within 4 weeks of
the Screening Visit: prednisone, opiates, baclofen, gabapentin,
pregabalin, thalidomide, amitriptyline, inhaled corticosteroids, or inhaled
bronchodilators
12. Use of ACE inhibitors or cromolyn sodium within 4 weeks of the
Screening Visit
13. Females who are pregnant or breastfeeding, or if of child-bearing
potential unwilling to practice acceptable means of birth control during
the study (e.g., abstinence, combination barrier and spermicide,
hormonal, or male partner sterilization)
14. History of hypersensitivity or intolerance to cromolyn sodium or its inactive ingredients

E.5 End points

E.5.1

Primary end point(s)

Primary endpoint:
• Change from baseline at the end of treatment in 24-hour average cough count

E.5.1.1

Timepoint(s) of evaluation of this end point

Week 12.

E.5.2

Secondary end point(s)

Secondary endpoints:
• Change from baseline at the end of treatment in cough severity as measured by VAS
• Change from baseline at the end of treatment in cough-specific QoL as measured by LCQ
• Proportion of responders with a minimum of 20% decrease from baseline at the end of
treatment in 24-hour average cough count
• Change from baseline at the end of treatment in daytime average cough count
• Change from baseline at the end of treatment in nighttime average cough count
• Change from baseline at the end of treatment in ILD-specific QoL as measured by K-BILD
• Change from baseline at the end of treatment in respiratory-related QoL as measured by SGRQ
• Change from baseline at the end of treatment in dyspnea score as measured by SOBQ
• Change from baseline at the end of treatment in 6MWT
• Change from baseline at the end of treatment in FVC
• Proportion of subjects with no decline (i.e., < 5% decline), 5% - 10% decline, and > 10%
decline in FVC % predicted at the end of treatment
• Change from baseline at the end of treatment in airway and lung volumes as measured by FRI
• Change from baseline at the end of treatment in average daily oxygen use
• Change from baseline at the end of treatment in exploratory biomarkers

E.5.2.1

Timepoint(s) of evaluation of this end point

Week 12.

E.6 and E.7 Scope of the trial

E.6

Scope of the trial

E.6.1

Diagnosis

E.6.2

Prophylaxis

E.6.3

Therapy

Yes

E.6.4

Safety

Yes

E.6.5

Efficacy

Yes

E.6.6

Pharmacokinetic

Yes

E.6.7

Pharmacodynamic

E.6.8

Bioequivalence

E.6.9

Dose response

Yes

E.6.10

Pharmacogenetic

E.6.11

Pharmacogenomic

E.6.12

Pharmacoeconomic

E.6.13

Others

E.7

Trial type and phase

E.7.1

Human pharmacology (Phase I)

E.7.1.1

First administration to humans

E.7.1.2

Bioequivalence study

E.7.1.3

Other

E.7.1.3.1

Other trial type description

E.7.2

Therapeutic exploratory (Phase II)

Yes

E.7.3

Therapeutic confirmatory (Phase III)

E.7.4

Therapeutic use (Phase IV)

E.8 Design of the trial

E.8.1

Controlled

Yes

E.8.1.1

Randomised

Yes

E.8.1.2

Open

E.8.1.3

Single blind

E.8.1.4

Double blind

Yes

E.8.1.5

Parallel group

Yes

E.8.1.6

Cross over

E.8.1.7

Other

E.8.2

Comparator of controlled trial

E.8.2.1

Other medicinal product(s)

E.8.2.2

Placebo

Yes

E.8.2.3

Other

E.8.2.4

Number of treatment arms in the trial

E.8.3

The trial involves single site in the Member State concerned

Yes

E.8.4

The trial involves multiple sites in the Member State concerned

E.8.5

The trial involves multiple Member States

Yes

E.8.5.1

Number of sites anticipated in the EEA

E.8.6 Trial involving sites outside the EEA

E.8.6.1

Trial being conducted both within and outside the EEA

Yes

E.8.6.2

Trial being conducted completely outside of the EEA

E.8.6.3

If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned

Australia

Belgium

Canada

Czech Republic

Germany

Italy

Netherlands

New Zealand

Turkey

United Kingdom

United States

E.8.7

Trial has a data monitoring committee

E.8.8

Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial

The end of the study will be determined by the last visit of the last
subject randomized.

E.8.9 Initial estimate of the duration of the trial

E.8.9.1

In the Member State concerned years

E.8.9.1

In the Member State concerned months

E.8.9.1

In the Member State concerned days

E.8.9.2

In all countries concerned by the trial years

E.8.9.2

In all countries concerned by the trial months

E.8.9.2

In all countries concerned by the trial days

F. Population of Trial Subjects

F.1 Age Range

F.1.1

Trial has subjects under 18

F.1.1.1

In Utero

F.1.1.2

Preterm newborn infants (up to gestational age < 37 weeks)

F.1.1.3

Newborns (0-27 days)

F.1.1.4

Infants and toddlers (28 days-23 months)

F.1.1.5

Children (2-11years)

F.1.1.6

Adolescents (12-17 years)

F.1.2

Adults (18-64 years)

Yes

F.1.2.1

Number of subjects for this age range:

180

F.1.3

Elderly (>=65 years)

Yes

F.1.3.1

Number of subjects for this age range:

100

F.2 Gender

F.2.1

Female

Yes

F.2.2

Male

Yes

F.3 Group of trial subjects

F.3.1

Healthy volunteers

F.3.2

Patients

Yes

F.3.3

Specific vulnerable populations

Yes

F.3.3.1

Women of childbearing potential not using contraception

F.3.3.2

Women of child-bearing potential using contraception

Yes

F.3.3.3

Pregnant women

F.3.3.4

Nursing women

F.3.3.5

Emergency situation

F.3.3.6

Subjects incapable of giving consent personally

F.3.3.7

Others

F.4 Planned number of subjects to be included

F.4.1

In the member state

F.4.2

For a multinational trial

F.4.2.1

In the EEA

F.4.2.2

In the whole clinical trial

180

F.5

Plans for treatment or care after the subject has ended the participation in the trial (if it is different from the expected normal treatment of that condition)

None.

G. Investigator Networks to be involved in the Trial

N. Review by the Competent Authority or Ethics Committee in the country concerned

Competent Authority Decision

Authorised

Date of Competent Authority Decision

2019-05-02

Ethics Committee Opinion of the trial application

Favourable

Ethics Committee Opinion: Reason(s) for unfavourable opinion

Date of Ethics Committee Opinion

2019-05-15

P. End of Trial
P.	End of Trial Status	Completed
P.	Date of the global end of the trial	2020-05-29

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Orphan Designation Number:
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