Ignite Creation Date:
2024-05-05 @ 10:23 AM
Last Modification Date:
2024-10-26 @ 9:02 AM
Study NCT ID:
NCT00000641
Status:
COMPLETED
Last Update Posted:
2021-11-03
First Post:
1999-11-02
Brief Title:
A Phase IIIII Trial of Rifampin Ciprofloxacin Clofazimine Ethambutol and Amikacin in the Treatment of Disseminated Mycobacterium Avium Infection in HIV-Infected Individuals
Sponsor:
National Institute of Allergy and Infectious Diseases NIAID
Organization:
National Institute of Allergy and Infectious Diseases NIAID
Study Overview
Official Title:
A Phase IIIII Trial of Rifampin Ciprofloxacin Clofazimine Ethambutol and Amikacin in the Treatment of Disseminated Mycobacterium Avium Infection in HIV-Infected Individuals
Status:
COMPLETED
Status Verified Date:
2021-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To compare the effectiveness and toxicity of two combination drug treatment programs for the treatment of disseminated Mycobacterium avium infection in HIV seropositive patients Per 030692 amendment to evaluate the efficacy of azithromycin when given in conjunction with either ethambutol or clofazimine as maintenance therapy Disseminated M avium infection is the most common systemic bacterial infection complicating AIDS in the United States The prognosis of patients with disseminated M avium is extremely poor particularly when it follows other opportunistic infections or is associated with anemia Test tube studies and clinical data indicate that the best treatment program may include clofazimine ethambutol a rifamycin derivative and ciprofloxacin Test tube and animal studies indicate that amikacin is a bactericidal bacteria destroying drug that works better when used with ciprofloxacin Its role in treatment programs is a key issue because of toxicity and because it must be administered parenterally by injection or intravenously
Detailed Description:
Disseminated M avium infection is the most common systemic bacterial infection complicating AIDS in the United States The prognosis of patients with disseminated M avium is extremely poor particularly when it follows other opportunistic infections or is associated with anemia Test tube studies and clinical data indicate that the best treatment program may include clofazimine ethambutol a rifamycin derivative and ciprofloxacin Test tube and animal studies indicate that amikacin is a bactericidal bacteria destroying drug that works better when used with ciprofloxacin Its role in treatment programs is a key issue because of toxicity and because it must be administered parenterally by injection or intravenously
Patients undergo an initial 2-week observation period days 1 - 14 during which time baseline evaluations are performed and type and severity of symptoms are monitored Eligible patients are randomized on day 15 to one of two treatment programs 1 ciprofloxacin clofazimine ethambutol and rifampin all taken orally or 2 the same four drugs plus amikacin Only patients for whom blood cultures obtained on either day 1 or day 1415 are positive by week 6 continue on study drugs Patients receive combination therapy for 24 weeks Patients may have an indwelling central venous catheter in place for long-term administration of intravenous drug PER 030692 AMENDMENT Newly enrolled patients who demonstrate a complete or partial clinical response at the end of study week 10 8 weeks of drug therapy discontinue their current regimen and begin maintenance therapy with azithromycin plus either ethambutol or clofazimine for an additional 24 weeks Patients who do not demonstrate a response at study week 10 are discontinued from all study therapy Patients enrolled on earlier versions of the protocol who have surpassed study week 16 14 weeks of drug therapy continue treatment with their originally assigned regimen through study week 26 those who have not surpassed study week 16 are considered for inclusion in the maintenance phase of the study
Patients undergo an initial 2-week observation period days 1 - 14 during which time baseline evaluations are performed and type and severity of symptoms are monitored Eligible patients are randomized on day 15 to one of two treatment programs 1 ciprofloxacin clofazimine ethambutol and rifampin all taken orally or 2 the same four drugs plus amikacin Only patients for whom blood cultures obtained on either day 1 or day 1415 are positive by week 6 continue on study drugs Patients receive combination therapy for 24 weeks Patients may have an indwelling central venous catheter in place for long-term administration of intravenous drug PER 030692 AMENDMENT Newly enrolled patients who demonstrate a complete or partial clinical response at the end of study week 10 8 weeks of drug therapy discontinue their current regimen and begin maintenance therapy with azithromycin plus either ethambutol or clofazimine for an additional 24 weeks Patients who do not demonstrate a response at study week 10 are discontinued from all study therapy Patients enrolled on earlier versions of the protocol who have surpassed study week 16 14 weeks of drug therapy continue treatment with their originally assigned regimen through study week 26 those who have not surpassed study week 16 are considered for inclusion in the maintenance phase of the study
Study Oversight
Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 11110 | REGISTRY | DAIDS ES Registry Number | None |