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The Safety of Different Dose Levels of Zidovudine in HIV-Infected Children

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Zidovudine
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Acquired Immunodeficiency Syndrome, Zidovudine

Eligibility Criteria

3 Months - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria Concurrent Medication: AMENDED: 03-19-91 Prophylaxis for PCP is recommended according to current practice guidelines. As per published recommendations, primary prophylaxis with TMP / SMX on a M-T-W basis is encouraged. Allowed: Immunoglobulin therapy as single dose exposure prophylaxis or for children with hypogammaglobulinemia. Trimethoprim / sulfamethoxazole (TMP / SMX) and parenteral or aerosolized pentamidine for prophylaxis for Pneumocystis carinii pneumonia for children with AIDS and/or CD4+ counts = or < 500 cells/mm3. Systemic ketoconazole and acyclovir, or oral nystatin for acute therapy. Aerosol ribavirin for short-term treatment of acute respiratory syncytial virus (RSV). AMENDED: 9/17/90 enrollment is limited to children < 6 years of age. Original design: Patients must have the following: Parent or guardian available to give written informed consent. Laboratory evidence of HIV infection. Children < 15 months of age, with CD4+ cell count > 500 cells/mm3, who are thought to have acquired HIV through perinatal transmission and whose only laboratory evidence of HIV infection is a positive antibody test, must also have one or more of the laboratory criteria described in Disease Status AND one or more of the disease criteria that are required of children > 15 months old with CD4+ cell counts > 500 cells/mm3. Prior Medication: Allowed: Aerosol ribavirin. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Previous AIDS-defining opportunistic infection or neoplasms as specified by the CDC surveillance criteria for AIDS. Previous unexplained recurrent, serious bacterial infections (two or more within a 2-year period) including sepsis, meningitis, pneumonia, abscess of an internal organ, and bone/joint infections caused by Haemophilus, Streptococcus, or other pyogenic bacteria. Qualifying for entrance criteria to zidovudine (AZT) + or - gammaglobulin (ACTG 051). Encephalopathy. Failure to thrive (defined as a child who crosses two percentile lines on the growth chart or child who is < fifth percentile and does not follow curve) and/or oral candidiasis for at least 2 months despite appropriate topical therapy. Lymphocytic interstitial pneumonitis (LIP) with steroid dependency or requiring supplemental oxygen. Preexisting malignancies. Concurrent Medication: AMENDED: 03-19-91 Prophylaxis with antiviral or antifungals agents, except for PCP prophylaxis is prohibited. Drugs that are metabolized by hepatic glucuronidation should be used with caution. Excluded: Prophylaxis for oral candidiasis or otitis media or other infections (sinusitis, urinary tract infections). Immunoglobulin therapy not specifically allowed. Ketoconazole, acyclovir, or nystatin for prophylaxis. Drugs that are metabolized by hepatic glucuronidation and might alter metabolism of zidovudine (AZT). Patients with the following are excluded: Previous AIDS-defining opportunistic infection or neoplasms as specified by the CDC surveillance criteria for AIDS. Previous unexplained recurrent, serious bacterial infections (two or more within a 2-year period) including sepsis, meningitis, pneumonia, abscess of an internal organ, and bone/joint infections caused by Haemophilus, Streptococcus, or other pyogenic bacteria. Qualifying for entrance criteria to zidovudine (AZT) + or - gammaglobulin (ACTG 051). Encephalopathy. Failure to thrive (defined as a child who crosses two percentile lines on the growth chart or child who is < fifth percentile and does not follow curve) and/or oral candidiasis for at least 2 months despite appropriate topical therapy. Lymphocytic interstitial pneumonitis (LIP) with steroid dependency or requiring supplemental oxygen. Preexisting malignancies. Prior Medication: Excluded within 2 weeks of study entry: Any other experimental therapy or drugs that cause prolonged neutropenia or significant nephrotoxicity. Excluded within 1 month of study entry: Antiretroviral agents. Immunomodulating agents including immunoglobulin, interferon, isoprinosine, and IL-2. Excluded within 2 months of study entry: Systemic ribavirin for retroviral therapy. Prior Treatment: Excluded within 1 month of study entry: Lymphocyte or red blood cell transfusions. Active alcohol or drug abuse.

Sites / Locations

  • Kaiser Permanente / UCLA Med Ctr
  • Long Beach Memorial (Pediatric)
  • Children's Hosp of Los Angeles/UCLA Med Ctr
  • Los Angeles County - USC Med Ctr
  • Cedars Sinai / UCLA Med Ctr
  • UCLA Med Ctr / Pediatric
  • Children's Hosp of Oakland
  • Univ of California / San Diego Treatment Ctr
  • Northern California Pediatric AIDS Treatment Ctr / UCSF
  • Univ of Connecticut Health Ctr / Pediatrics
  • Children's Natl Med Ctr
  • Ctr for Special Immunology
  • Univ of Miami School of Medicine
  • Emory Univ School of Medicine
  • Cook County Hosp
  • Univ of Illinois College of Medicine
  • Chicago Children's Memorial Hosp
  • Univ of Maryland at Baltimore / Univ Med Ctr
  • Johns Hopkins Hosp - Pediatric
  • Children's Hosp of Boston
  • Boston Med Ctr
  • Univ of Massachusetts Med Ctr
  • Children's Hosp of New Jersey / UMDNJ - New Jersey Med Schl
  • Lincoln Hosp Ctr / Pediatrics
  • Bronx Lebanon Hosp Ctr
  • Albert Einstein College of Medicine
  • SUNY / Health Sciences Ctr at Brooklyn / Pediatrics
  • Jewish Hosp Ctr of Long Island / Pediatrics
  • Schneider Children's Hosp / Long Island Jewish Med Ctr
  • Beth Israel Med Ctr / Pediatrics
  • Bellevue Hosp / New York Univ Med Ctr
  • Cornell Univ Med College
  • Saint Luke's - Roosevelt Hosp Ctr
  • Metropolitan Hosp Ctr
  • Mount Sinai Med Ctr
  • Columbia Univ Babies' Hosp
  • Harlem Hosp Ctr
  • Univ of Rochester Medical Center
  • Westchester Hosp / New York Med College / Pediatrics
  • Univ of North Carolina
  • Duke Univ Med Ctr
  • Bowman Gray School of Medicine / North Carolina Baptist Hosp
  • Holmes Hosp / Univ of Cincinnati Med Ctr
  • Columbus Children's Hosp
  • Hemophilia Ctr of Western PA / Univ of Pittsburgh
  • Julio Arroyo
  • Hermann Hosp / Univ Texas Health Science Ctr
  • Texas Children's Hosp / Baylor Univ
  • Ramon Ruiz Arnau Univ Hosp / Pediatrics
  • San Juan City Hosp
  • UPR Children's Hosp / San Juan City Hosp

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 28, 2021
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Glaxo Wellcome
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1. Study Identification

Unique Protocol Identification Number
NCT00000983
Brief Title
The Safety of Different Dose Levels of Zidovudine in HIV-Infected Children
Official Title
A Randomized Blinded Trial To Evaluate the Safety and Tolerance of High Versus Low Dose Zidovudine Administered to Children With Human Immunodeficiency Virus
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 1994 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators
Glaxo Wellcome

4. Oversight

5. Study Description

Brief Summary
To evaluate and compare differences in tolerance and side effects associated with two different dosages of zidovudine (AZT) when used to treat children with HIV infection. Other goals are to evaluate and compare the degree of change in neurodevelopmental disease and determine whether there are differences in the rate and degree of toxicities associated with one versus the other dosage. AZT has been shown to decrease the death rate and frequency of opportunistic infections in certain adult patients with symptomatic HIV infection. Thus, it is likely that symptomatic HIV infected children may also benefit from AZT. Studies of the safety and pharmacokinetics (blood levels) in children have indicated that AZT can be given to children in doses that can be tolerated and that can be assumed to be therapeutic. Those currently taking care of infected children no longer feel it is ethical to conduct an AZT/placebo (inactive substance) trial. In addition, given the information learned from studies of adult patients that shows effectiveness of AZT at lower doses, experience with an equivalent lower dose in children needs to be studied.
Detailed Description
AZT has been shown to decrease the death rate and frequency of opportunistic infections in certain adult patients with symptomatic HIV infection. Thus, it is likely that symptomatic HIV infected children may also benefit from AZT. Studies of the safety and pharmacokinetics (blood levels) in children have indicated that AZT can be given to children in doses that can be tolerated and that can be assumed to be therapeutic. Those currently taking care of infected children no longer feel it is ethical to conduct an AZT/placebo (inactive substance) trial. In addition, given the information learned from studies of adult patients that shows effectiveness of AZT at lower doses, experience with an equivalent lower dose in children needs to be studied. All participants are randomized to receive AZT at 1 of 2 doses. Patients are stratified according to whether CD4 cell counts are > or < 500 cells/mm3 as well as whether symptoms are mild to moderate or if patients have lymphocytic interstitial pneumonitis (LIP). Medication is dispensed every other week for the first 8 weeks and monthly until week 104, then either monthly or every 3 months. Safety and effectiveness of the treatment program are evaluated at 6-month intervals to assess whether it is appropriate to continue the study as originally designed. Patients are evaluated every 2 weeks for the first 8 weeks, monthly until week 104, every 3 months until week 208, and then every 6 months thereafter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Acquired Immunodeficiency Syndrome, Zidovudine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Enrollment
400 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Zidovudine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Concurrent Medication: AMENDED: 03-19-91 Prophylaxis for PCP is recommended according to current practice guidelines. As per published recommendations, primary prophylaxis with TMP / SMX on a M-T-W basis is encouraged. Allowed: Immunoglobulin therapy as single dose exposure prophylaxis or for children with hypogammaglobulinemia. Trimethoprim / sulfamethoxazole (TMP / SMX) and parenteral or aerosolized pentamidine for prophylaxis for Pneumocystis carinii pneumonia for children with AIDS and/or CD4+ counts = or < 500 cells/mm3. Systemic ketoconazole and acyclovir, or oral nystatin for acute therapy. Aerosol ribavirin for short-term treatment of acute respiratory syncytial virus (RSV). AMENDED: 9/17/90 enrollment is limited to children < 6 years of age. Original design: Patients must have the following: Parent or guardian available to give written informed consent. Laboratory evidence of HIV infection. Children < 15 months of age, with CD4+ cell count > 500 cells/mm3, who are thought to have acquired HIV through perinatal transmission and whose only laboratory evidence of HIV infection is a positive antibody test, must also have one or more of the laboratory criteria described in Disease Status AND one or more of the disease criteria that are required of children > 15 months old with CD4+ cell counts > 500 cells/mm3. Prior Medication: Allowed: Aerosol ribavirin. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Previous AIDS-defining opportunistic infection or neoplasms as specified by the CDC surveillance criteria for AIDS. Previous unexplained recurrent, serious bacterial infections (two or more within a 2-year period) including sepsis, meningitis, pneumonia, abscess of an internal organ, and bone/joint infections caused by Haemophilus, Streptococcus, or other pyogenic bacteria. Qualifying for entrance criteria to zidovudine (AZT) + or - gammaglobulin (ACTG 051). Encephalopathy. Failure to thrive (defined as a child who crosses two percentile lines on the growth chart or child who is < fifth percentile and does not follow curve) and/or oral candidiasis for at least 2 months despite appropriate topical therapy. Lymphocytic interstitial pneumonitis (LIP) with steroid dependency or requiring supplemental oxygen. Preexisting malignancies. Concurrent Medication: AMENDED: 03-19-91 Prophylaxis with antiviral or antifungals agents, except for PCP prophylaxis is prohibited. Drugs that are metabolized by hepatic glucuronidation should be used with caution. Excluded: Prophylaxis for oral candidiasis or otitis media or other infections (sinusitis, urinary tract infections). Immunoglobulin therapy not specifically allowed. Ketoconazole, acyclovir, or nystatin for prophylaxis. Drugs that are metabolized by hepatic glucuronidation and might alter metabolism of zidovudine (AZT). Patients with the following are excluded: Previous AIDS-defining opportunistic infection or neoplasms as specified by the CDC surveillance criteria for AIDS. Previous unexplained recurrent, serious bacterial infections (two or more within a 2-year period) including sepsis, meningitis, pneumonia, abscess of an internal organ, and bone/joint infections caused by Haemophilus, Streptococcus, or other pyogenic bacteria. Qualifying for entrance criteria to zidovudine (AZT) + or - gammaglobulin (ACTG 051). Encephalopathy. Failure to thrive (defined as a child who crosses two percentile lines on the growth chart or child who is < fifth percentile and does not follow curve) and/or oral candidiasis for at least 2 months despite appropriate topical therapy. Lymphocytic interstitial pneumonitis (LIP) with steroid dependency or requiring supplemental oxygen. Preexisting malignancies. Prior Medication: Excluded within 2 weeks of study entry: Any other experimental therapy or drugs that cause prolonged neutropenia or significant nephrotoxicity. Excluded within 1 month of study entry: Antiretroviral agents. Immunomodulating agents including immunoglobulin, interferon, isoprinosine, and IL-2. Excluded within 2 months of study entry: Systemic ribavirin for retroviral therapy. Prior Treatment: Excluded within 1 month of study entry: Lymphocyte or red blood cell transfusions. Active alcohol or drug abuse.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
M Brady
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
P Weintrub
Official's Role
Study Chair
Facility Information:
Facility Name
Kaiser Permanente / UCLA Med Ctr
City
Downey
State/Province
California
ZIP/Postal Code
902422814
Country
United States
Facility Name
Long Beach Memorial (Pediatric)
City
Long Beach
State/Province
California
ZIP/Postal Code
90801
Country
United States
Facility Name
Children's Hosp of Los Angeles/UCLA Med Ctr
City
Los Angeles
State/Province
California
ZIP/Postal Code
900276016
Country
United States
Facility Name
Los Angeles County - USC Med Ctr
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Cedars Sinai / UCLA Med Ctr
City
Los Angeles
State/Province
California
ZIP/Postal Code
900481804
Country
United States
Facility Name
UCLA Med Ctr / Pediatric
City
Los Angeles
State/Province
California
ZIP/Postal Code
900951752
Country
United States
Facility Name
Children's Hosp of Oakland
City
Oakland
State/Province
California
ZIP/Postal Code
946091809
Country
United States
Facility Name
Univ of California / San Diego Treatment Ctr
City
San Diego
State/Province
California
ZIP/Postal Code
921036325
Country
United States
Facility Name
Northern California Pediatric AIDS Treatment Ctr / UCSF
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Univ of Connecticut Health Ctr / Pediatrics
City
Farmington
State/Province
Connecticut
ZIP/Postal Code
06032
Country
United States
Facility Name
Children's Natl Med Ctr
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States
Facility Name
Ctr for Special Immunology
City
Fort Lauderdale
State/Province
Florida
ZIP/Postal Code
33308
Country
United States
Facility Name
Univ of Miami School of Medicine
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
Emory Univ School of Medicine
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30303
Country
United States
Facility Name
Cook County Hosp
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Univ of Illinois College of Medicine
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
Chicago Children's Memorial Hosp
City
Chicago
State/Province
Illinois
ZIP/Postal Code
606143394
Country
United States
Facility Name
Univ of Maryland at Baltimore / Univ Med Ctr
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
Johns Hopkins Hosp - Pediatric
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
212874933
Country
United States
Facility Name
Children's Hosp of Boston
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
021155724
Country
United States
Facility Name
Boston Med Ctr
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Facility Name
Univ of Massachusetts Med Ctr
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Facility Name
Children's Hosp of New Jersey / UMDNJ - New Jersey Med Schl
City
Newark
State/Province
New Jersey
ZIP/Postal Code
071072198
Country
United States
Facility Name
Lincoln Hosp Ctr / Pediatrics
City
Bronx
State/Province
New York
ZIP/Postal Code
10451
Country
United States
Facility Name
Bronx Lebanon Hosp Ctr
City
Bronx
State/Province
New York
ZIP/Postal Code
10456
Country
United States
Facility Name
Albert Einstein College of Medicine
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Facility Name
SUNY / Health Sciences Ctr at Brooklyn / Pediatrics
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11203
Country
United States
Facility Name
Jewish Hosp Ctr of Long Island / Pediatrics
City
Jamaica
State/Province
New York
ZIP/Postal Code
11432
Country
United States
Facility Name
Schneider Children's Hosp / Long Island Jewish Med Ctr
City
New Hyde Park
State/Province
New York
ZIP/Postal Code
11042
Country
United States
Facility Name
Beth Israel Med Ctr / Pediatrics
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
Facility Name
Bellevue Hosp / New York Univ Med Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
Cornell Univ Med College
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Saint Luke's - Roosevelt Hosp Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10025
Country
United States
Facility Name
Metropolitan Hosp Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
Mount Sinai Med Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10029
Country
United States
Facility Name
Columbia Univ Babies' Hosp
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Harlem Hosp Ctr
City
New York
State/Province
New York
ZIP/Postal Code
10037
Country
United States
Facility Name
Univ of Rochester Medical Center
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States
Facility Name
Westchester Hosp / New York Med College / Pediatrics
City
Valhalla
State/Province
New York
ZIP/Postal Code
10595
Country
United States
Facility Name
Univ of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
275997215
Country
United States
Facility Name
Duke Univ Med Ctr
City
Durham
State/Province
North Carolina
ZIP/Postal Code
277103499
Country
United States
Facility Name
Bowman Gray School of Medicine / North Carolina Baptist Hosp
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27103
Country
United States
Facility Name
Holmes Hosp / Univ of Cincinnati Med Ctr
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
452670405
Country
United States
Facility Name
Columbus Children's Hosp
City
Columbus
State/Province
Ohio
ZIP/Postal Code
432052696
Country
United States
Facility Name
Hemophilia Ctr of Western PA / Univ of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15219
Country
United States
Facility Name
Julio Arroyo
City
West Columbia
State/Province
South Carolina
ZIP/Postal Code
29169
Country
United States
Facility Name
Hermann Hosp / Univ Texas Health Science Ctr
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Texas Children's Hosp / Baylor Univ
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Ramon Ruiz Arnau Univ Hosp / Pediatrics
City
Bayamon
ZIP/Postal Code
00619
Country
Puerto Rico
Facility Name
San Juan City Hosp
City
San Juan
ZIP/Postal Code
009367344
Country
Puerto Rico
Facility Name
UPR Children's Hosp / San Juan City Hosp
City
San Juan
ZIP/Postal Code
00936
Country
Puerto Rico

12. IPD Sharing Statement

Citations:
PubMed Identifier
9041402
Citation
Lathey JL, Marschner IC, Kabat B, Spector SA. Deterioration of detectable human immunodeficiency virus serum p24 antigen in samples stored for batch testing. J Clin Microbiol. 1997 Mar;35(3):631-5. doi: 10.1128/jcm.35.3.631-635.1997.
Results Reference
background
PubMed Identifier
7699053
Citation
Fiscus SA, Welles SL, Spector SA, Lathey JL. Length of incubation time for human immunodeficiency virus cultures. J Clin Microbiol. 1995 Jan;33(1):246-7. doi: 10.1128/jcm.33.1.246-247.1995.
Results Reference
background
PubMed Identifier
8627060
Citation
Brady MT, McGrath N, Brouwers P, Gelber R, Fowler MG, Yogev R, Hutton N, Bryson YJ, Mitchell CD, Fikrig S, Borkowsky W, Jimenez E, McSherry G, Rubinstein A, Wilfert CM, McIntosh K, Elkins MM, Weintrub PS. Randomized study of the tolerance and efficacy of high- versus low-dose zidovudine in human immunodeficiency virus-infected children with mild to moderate symptoms (AIDS Clinical Trials Group 128). Pediatric AIDS Clinical Trials Group. J Infect Dis. 1996 May;173(5):1097-106. doi: 10.1093/infdis/173.5.1097.
Results Reference
background
Citation
Brady M, McGrath N, Brouwers P, Gelber R, Fowler M, Weintrub P. Controlled trial of tolerance and efficacy of zidovudine (ZDV) at standard and low dose in children (ACTG 128). The Pediatric AIDS Clinical Trials Group. Int Conf AIDS. 1994 Aug 7-12;10(1):79 (abstract no 268B)
Results Reference
background
Citation
Parent D, Ellner J, Hafner R, Williams M, Jacobs P, Hojczyk P. A phase II/III trial of Rifampin (RIF) Ciprofloxach (CIPRO), Clofazimine (CLOF), Ethambutol (ETH), +/- Amikacin (AK) in the treatment (RX) of Disseminated Mycobacterium avium (MA) infection in HIV-infected individuals (PTS). Natl Conf Hum Retroviruses Relat Infect (2nd). 1995 Jan 29-Feb 2:56
Results Reference
background
PubMed Identifier
21037891
Citation
Perrier M, Schwarz T, Gonzalez O, Brounts S. Squamous cell carcinoma invading the right temporomandibular joint in a Belgian mare. Can Vet J. 2010 Aug;51(8):885-7.
Results Reference
background

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The Safety of Different Dose Levels of Zidovudine in HIV-Infected Children

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