Heart Failure Clinical Trial

Phase 1 Safety and Pharmacokinetic Study of AI-700 in Patients With Diminished DLCO and COPD and/or CHF

Summary

This study was conducted to evaluate the safety and pharmacokinetics of an echocardiographic contrast agent, AI-700, in patients with moderate to severe chronic obstructive pulmonary disease (COPD) and/or congestive heart failure (CHF).

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Full Description

In ongoing clinical trials, AI-700 is currently being evaluated for its value to provide enhanced echocardiography to detect CAD. The patient population is comprised of those patients who have chest pain and are being evaluated for inducible ischemia. This population may include patients with compromised pulmonary function due to COPD or CHF. This study was to evaluate the safety of AI-700 in these patients.

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Eligibility Criteria

Study is for people with:

Heart Failure

Phase:

Phase 1

Study ID:

NCT00156780

Recruitment Status:

Completed

Sponsor:

Acusphere

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There is 1 Location for this study

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Acusphere, Inc.
Watertown Massachusetts, 02472, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 1

Study ID:

NCT00156780

Recruitment Status:

Completed

Sponsor:


Acusphere

How clear is this clinincal trial information?

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