A Trial to Evaluate the Safety of Long Term Treatment With Nintedanib in Patients With Scleroderma Related Lung Fibrosis.



Status:Recruiting
Conditions:Pulmonary, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - Any
Updated:4/4/2019
Start Date:November 27, 2017
End Date:July 31, 2021
Contact:Boehringer Ingelheim
Email:clintriage.rdg@boehringer-ingelheim.com
Phone:1-800-243-0127

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An Open-label Extension Trial of the Long Term Safety of Nintedanib in Patients With 'Systemic Sclerosis Associated Interstitial Lung Disease' (SSc-ILD)

The main objective is to assess long term safety of treatment with oral nintedanib in
patients with Systemic Sclerosis associated Interstitial Lung Disease (SSc-ILD).


Inclusion Criteria:

- Patients who completed the parent trial 1199.214/1199-0340 per protocol and did not
permanently discontinue study treatment

- Signed and dated written informed consent in accordance with International Conference
on Harmonisation - Good Clinical Practice (ICH-GCP) and local legislation prior to
admission to the trial

- Women of childbearing potential must be ready and able to use highly effective methods
of birth control per ICH M3 (R2) that result in a low failure rate of less than 1% per
year when used consistently and correctly as well as one barrier method for 28 days
prior to nintedanib treatment initiation, during the trial and for 3 months after last
intake of nintedanib.

- Further inclusion criteria apply

Exclusion Criteria:

- Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT) > 3 x Upper Limit of
Normal (ULN)

- Bilirubin > 2 x ULN

- Creatinine clearance <30 mL/min calculated by Cockcroft-Gault formula.

- Clinically relevant anaemia at investigators discretion.

- Bleeding risk, any of the following

- Known genetic predisposition to bleeding according to the judgement of the
investigator

- Patients who require

- Fibrinolysis, full-dose therapeutic anticoagulation

- High dose antiplatelet therapy.

- Hemorrhagic central nervous system (CNS) event after completion of the parent
trial 1199.214/1199-0340

- Any of the following after last treatment of 1199.214/1199-0340:

- Haemoptysis or haematuria

- Active gastro-intestinal bleeding or Gastrointestinal (GI) - ulcers

- Gastric antral vascular ectasia (GAVE)

- Major injury or surgery

- Coagulation parameters: International normalised ratio (INR) >2, prolongation of
prothrombin time (PT) and partial thromboplastin time (PTT) by >1.5 x ULN at
Visit 1.

- New major thrombo-embolic events developed after completion of the parent trial
1199.214/1199-0340:

- Stroke;

- Deep vein thrombosis;

- Pulmonary embolism;

- Myocardial infarction.

- Major surgery performed within the next 3 months

- Time period > 12 weeks between last drug intake in 1199.214 or > 1 week between last
nintedanib intake in trial 1199-0340 and Visit 2 of this trial

- Usage of any investigational drug after completion of 1199.214/1199-0340 or planned
usage of an investigational drug during the course of this trial.

- A disease or condition which may put the patient at risk because of participation in
this trial (e.g. clinically relevant intestinal pseudoobstruction) or limit the
patient's ability to participate in this trial

- Chronic alcohol or drug abuse or any condition that, in the investigator's opinion,
makes them an unreliable trial subject or unlikely to complete the trial

- Known hypersensitivity to the trial medication or its components (i.e. soya lecithin).

- Women who are pregnant, nursing, or who plan to become pregnant while in the trial

- Previous enrolment in this trial

- Further exclusion criteria apply
We found this trial at
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303 East Superior Street
Chicago, Illinois 60611
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1720 2nd Ave S
Birmingham, Alabama 35233
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72 East Concord Street
Boston, Massachusetts 02118
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9500 Euclid Avenue
Cleveland, Ohio 44106
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101 Jessup Hall
Iowa City, Iowa 52242
(319) 335-3500
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Los Angeles, California 90095
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Miami, Florida 33124
(305) 284-2211
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1211 Medical Center Dr
Nashville, Tennessee 37232
(615) 322-5000
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Seattle, Washington 98104
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Atlanta, Georgia 30322
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13001 E. 17th Pl
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1800 Orleans St.
Baltimore, Maryland 21287
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726 Avenida Luis María Campos
Buenos Aires, C1426
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171 Ashley Avenue
Charleston, South Carolina 29425
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2600 Clifton Ave
Cincinnati, Ohio 45267
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1801 Inwood Rd
Dallas, Texas 75390
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2301 Erwin Rd
Durham, North Carolina 27710
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Falls Church, Virginia 22042
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Houston, Texas 77030
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Jacksonville, Florida 32209
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3901 Rainbow Blvd
Kansas City, Kansas 66160
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9200 W Wisconsin Ave
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333 Cedar St
New Haven, Connecticut 06504
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535 E 70th St
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1428 Madison Ave
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1020 Walnut St
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3401 N Broad St
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200 First Street SW
Rochester, Minnesota 55905
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1 Shields Ave
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660 S Euclid Ave
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300 Pasteur Dr
Stanford, California 94305
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2801 W. Bancroft
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3700 O St NW
Washington, District of Columbia 20057
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