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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00744341
Other study ID # S320.2.011
Secondary ID 2008-003786-2000
Status Terminated
Phase Phase 2
First received August 28, 2008
Last updated September 16, 2010
Start date February 2009
Est. completion date January 2010

Study information

Verified date September 2010
Source Solvay Pharmaceuticals
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the efficacy and safety of IV SLV320 in acute heart failure patients with renal dysfunction.


Description:

The purpose of this study is to determine the efficacy and safety of IV SLV320 in acute heart failure patients with renal dysfunction.


Recruitment information / eligibility

Status Terminated
Enrollment 46
Est. completion date January 2010
Est. primary completion date January 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria Renal dysfunction defined as estimated eGFR of 20-80 mL/min; history of systolic or diastolic chronic heart failure of at least 14 days duration for which loop diuretic therapy has been prescribed; clinical evidence for volume overload; BNP = 500 pg/mL or NT-pro-BNP > 2000 pg/mL; hospitalization.

Exclusion Criteria Have low output syndrome, defined as having the need for treatment with I.V. inotropes or vasopressors; Need mechanical ventilation; Have significant stenotic valvular disease (severe aortic or mitral stenosis); Have myocardial infarction or hemodynamically destabilizing significant arrythmias (ventricular tachycardia, bradyarrythmias with slow ventricular rate [<45 bpm] or atrial fibrillation/flutter with a rapid ventricular response of >120 bpm), or electrocardiographic evidence of 2nd degree heart block (Mobitz Type II) or 3rd degree AV-block in the absence of a pacemaker, within 30 days of screening; Have acute myocarditis or hypertrophic obstructive, restrictive, or constrictive cardiomyopathy

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
SLV320
1.25mg i.v. bid
SLV320
3.75mg i.v. bid
SLV320
7.5mg i.v. bid
SLV320
15.0mg i.v. bid
Placebo


Locations

Country Name City State
Canada S320.2.011 Site # 601 Montreal
Chile S320.2.011 Site # 427 Santiago
Chile S320.2.011 Site # 433 Viña del Mar
Chile S320.2.011 Site # 434 Viña del Mar
Denmark S320.2.011 Site # 100 Aarhus
Denmark S320.2.011 Site # 102 Aarhus
Denmark S320.2.011 Site # 103 Esbjerg
Denmark S320.2.011 Site # 106 Frederiksberg
Denmark S320.2.011 Site # 105 Herning
Denmark S320.2.011 Site # 104 København
France S320.2.011 Site # 125 Dijon
France S320.2.011 Site # 123 Lille
France S320.2.011 Site # 121 Paris
France S320.2.011 Site # 124 Pessac
France S320.2.011 Site # 126 Pontoise
France S320.2.011 Site # 128 Toulouse
Germany S320.2.011 Site # 182 Bad Nauheim
Germany S320.2.011 Site # 187 Berlin
Germany S320.2.011 Site # 186 Frankfurt
Germany S320.2.011 Site # 180 Hannover
Germany S320.2.011 Site # 185 Limburg
Germany S320.2.011 Site # 190 Mannheim
Germany S320.2.011 Site # 188 Weiden
Italy S320.2.011 Site # 146 Aosta
Italy S320.2.011 Site # 145 Cremona
Italy S320.2.011 Site # 142 Genova
Italy S320.2.011 Site # 149 Milano
Italy S320.2.011 Site # 140 Modena
Italy S320.2.011 Site # 143 Orbassano
Poland S320.2.011 Site # 250 Bialystok
Poland S320.2.011 Site # 231 Inowroclaw
Poland S320.2.011 Site # 236 Krakow
Poland S320.2.011 Site # 249 Lodz
Poland S320.2.011 Site # 243 Olawa
Poland S320.2.011 Site # 251 Plock
Poland S320.2.011 Site # 240 Poznan
Poland S320.2.011 Site # 247 Przeworsk
Poland S320.2.011 Site # 242 Pulawy
Poland S320.2.011 Site # 239 Radom
Poland S320.2.011 Site # 232 Ruda Slaska
Poland S320.2.011 Site # 245 Starogard Gdanski
Poland S320.2.011 Site # 234 Torun
Poland S320.2.011 Site # 248 Torun
Poland S320.2.011 Site # 238 Tychy
Poland S320.2.011 Site # 233 Wroclaw
Romania S320.2.011 Site # 265 Baia Mare
Romania S320.2.011 Site # 262 Braila
Romania S320.2.011 Site # 260 Bucuresti
Romania S320.2.011 Site # 263 Bucuresti
Romania S320.2.011 Site # 267 Bucuresti
Romania S320.2.011 Site # 264 Suceava
Romania S320.2.011 Site # 261 Targoviste
Romania S320.2.011 Site # 266 Timisoara
Russian Federation S320.2.011 Site # 294 Kazan
Russian Federation S320.2.011 Site # 306 Krasnodar
Russian Federation S320.2.011 Site # 290 Moscow
Russian Federation S320.2.011 Site # 297 Moscow
Russian Federation S320.2.011 Site # 299 Moscow
Russian Federation S320.2.011 Site # 301 Moscow
Russian Federation S320.2.011 Site # 303 Moscow
Russian Federation S320.2.011 Site # 304 Moscow
Russian Federation S320.2.011 Site # 305 Moscow
Russian Federation S320.2.011 Site # 291 Saint-Petersburg
Russian Federation S320.2.011 Site # 292 Saint-Petersburg
Russian Federation S320.2.011 Site # 298 Saint-Petersburg
Russian Federation S320.2.011 Site # 302 Saint-Petersburg
Russian Federation S320.2.011 Site # 300 St. Petersburg
Russian Federation S320.2.011 Site # 293 Voronezh
Russian Federation S320.2.011 Site # 295 Yaroslavl
Ukraine S320.2.011 Site # 335 Dnipropetrovsk
Ukraine S320.2.011 Site # 332 Ivano-Frankivsk
Ukraine S320.2.011 Site # 334 Kharkiv
Ukraine S320.2.011 Site # 330 Kyiv
Ukraine S320.2.011 Site # 338 Kyiv
Ukraine S320.2.011 Site # 331 Lugansk
Ukraine S320.2.011 Site # 333 Lutsk
Ukraine S320.2.011 Site # 337 Odessa
United States S320.2.011 Site # 521 Akron Ohio
United States S320.2.011 Site # 548 Alameda California
United States S320.2.011 Site # 566 Banning California
United States S320.2.011 Site # 546 Biddeford Maine
United States S320.2.011 Site # 564 Bridgeport Connecticut
United States S320.2.011 Site # 541 Brooklyn New York
United States S320.2.011 Site # 513 Chicago Illinois
United States S320.2.011 Site # 510 Colombia South Carolina
United States S320.2.011 Site # 523 Dearborn Michigan
United States S320.2.011 Site # 534 Detroit Michigan
United States S320.2.011 Site # 558 Detroit Michigan
United States S320.2.011 Site # 505 Hollywood Florida
United States S320.2.011 Site # 511 Houston Texas
United States S320.2.011 Site # 561 Indianapolis Indiana
United States S320.2.011 Site # 551 Inglewood California
United States S320.2.011 Site # 507 Jacksonville Florida
United States S320.2.011 Site # 556 Manitowoc Wisconsin
United States S320.2.011 Site # 565 Milwaukee Wisconsin
United States S320.2.011 Site # 545 Nashville Tennessee
United States S320.2.011 Site # 504 Natchitoches Louisiana
United States S320.2.011 Site # 537 New York New York
United States S320.2.011 Site # 526 Owensboro Kentucky
United States S320.2.011 Site # 528 Philadelphia Pennsylvania
United States S320.2.011 Site # 532 Riverdale Georgia
United States S320.2.011 Site # 518 San Antonio Texas
United States S320.2.011 Site # 508 St. Louis Missouri
United States S320.2.011 Site # 527 Toledo Ohio
United States S320.2.011 Site # 519 Tullahoma Tennessee

Sponsors (1)

Lead Sponsor Collaborator
Solvay Pharmaceuticals

Countries where clinical trial is conducted

United States,  Canada,  Chile,  Denmark,  France,  Germany,  Italy,  Poland,  Romania,  Russian Federation,  Ukraine, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in serum creatinine from baseline to Day 14 Day 14 No
Secondary To compare four SLV320 doses to placebo on the change in the following variables: Dyspnea (Likert Scale and PDA scale), eGFR (MDRD Formula), Subject Global Clinical Assessment Score, Urine Osmolality, Serum Osmolality Up to Day 3 (Dyspnea); Up to Day 4 (Urine Osmolality); Up to Day 60 (eGFR, Subject Global Clinical Assessment Score, Serum Osmolality) No
Secondary To compare the effect of four I.V. doses of SLV320 with placebo using the trichotomous endpoint of treatment success, treatment failure, or no change Up to Day 14 No
Secondary To compare the effect of four I.V. doses of SLV320 with placebo on top of diuretic use Up to Day 3 No
Secondary To compare the effect of four I.V. doses of SLV320 with placebo using a composite endpoint of all-cause mortality, cardiovascular hospitalization or hospitalization for worsening renal function, in time to event and frequency Up to Day 180 Yes
Secondary To determine the pharmacokinetic profile of I.V. SLV320 Up to Day 3 No