NCT00001038

Brief Summary

PRIMARY: To evaluate the efficacy of valacyclovir hydrochloride (BW 256U87) in the prevention of cytomegalovirus (CMV) end-organ disease in HIV/CMV co-infected patients with CD4+ lymphocytes \< 100 cells/mm3. To assess the impact of BW 256U87, high-dose oral acyclovir and low-dose oral acyclovir on survival. SECONDARY: To evaluate the effect of BW 256U87 on quality of life, the safety of the drug administered concurrently with standard antiretroviral agents and other essential therapies for the treatment and prevention of opportunistic diseases, and the efficacy of BW 256U87 in suppressing activation of other herpesviruses. To evaluate serologic and virologic risk factors for the development of CMV disease, including assessment of HIV activation, and the risk of developing drug-resistant CMV, HSV, and VZV. Gastrointestinal absorption of acyclovir is not high enough to prevent CMV disease in patients with advanced HIV disease, although there is evidence that high doses of the drug may extend survival. Valacyclovir, a prodrug that is rapidly converted to acyclovir after oral administration, has a higher absorption rate and may therefore provide inhibitory activity against CMV.

Trial Health

98
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,200

participants targeted

Target at P75+ for phase_3

Geographic Reach
10 countries

35 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Primary Completion

Last participant's last visit for primary outcome

May 1, 1996

Completed
3.5 years until next milestone

First Submitted

Initial submission to the registry

November 2, 1999

Completed
1.8 years until next milestone

First Posted

Study publicly available on registry

August 31, 2001

Completed
Last Updated

March 1, 2011

Status Verified

February 1, 2011

First QC Date

November 2, 1999

Last Update Submit

February 28, 2011

Conditions

Keywords

Cytomegalovirus InfectionsAcquired Immunodeficiency SyndromeAntiviral Agents

Interventions

Eligibility Criteria

Age13 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Concurrent Medication:
  • Recommended:
  • PCP prophylaxis.
  • Allowed:
  • Any antiretroviral therapies available by prescription or through expanded access or Treatment IND programs, including combination or sequential use.
  • Chemotherapy for Kaposi's sarcoma, lymphoma, or other malignancies IF patient is hematologically stable for at least 30 days prior to study entry.
  • Discrete courses of oral or parenteral acyclovir for VZV or HSV infection, not to exceed 21 days per episode (may co-enroll on ACTG 169). For recurrent episodes, open-label acyclovir for a total of 60 days over a 12-month period is allowed. Study drug is interrupted.
  • Supportive therapies available by prescription, expanded access, or Treatment IND programs, such as G-CSF, GM-CSF, and erythropoietin.
  • Other medications necessary for the patient's welfare, at the discretion of the investigator.
  • Patients must have:
  • HIV infection or AIDS-defining conditions.
  • CD4+ count \< 100 cells/mm3.
  • IgG antibodies to CMV.
  • No active CMV disease or history of CMV end-organ disease.
  • Consent of parent or guardian if less than 18 years of age.
  • +10 more criteria

You may not qualify if:

  • Co-existing Condition:
  • Patients with the following symptoms and conditions are excluded:
  • Nausea or vomiting that precludes oral dosing.
  • Ocular media opacities that preclude adequate visualization of fundi.
  • Pregnancy.
  • Known hypersensitivity to acyclovir.
  • Known lactose intolerance.
  • Concurrent Medication:
  • Excluded:
  • Systemic interferons and immunomodulators (including CMV hyperimmune serum/globulin and chronic corticosteroids at doses in excess of physiologic replacement).
  • Probenecid.
  • Investigational or marketed agents with potential activity against CMV, herpes simplex, and/or Varicella zoster, EXCEPT as specifically allowed.
  • Patients with the following prior condition are excluded:
  • Pre-existing necrotizing retinopathy that may interfere with a subsequent diagnosis of CMV retinitis.
  • Prior Medication:
  • +3 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (35)

Birmingham Veterans Administration Med Ctr

Birmingham, Alabama, 35233, United States

Location

Los Angeles County - USC Med Ctr

Los Angeles, California, 90033, United States

Location

CARE Ctr / UCLA Med Ctr

Los Angeles, California, 900951793, United States

Location

Highland Gen Hosp / San Francisco Gen Hosp

Oakland, California, 946021018, United States

Location

Univ of California / San Diego Treatment Ctr

San Diego, California, 921036325, United States

Location

Kaiser Permanente Med Ctr

San Francisco, California, 94115, United States

Location

Univ of Colorado Health Sciences Ctr

Denver, Colorado, 80262, United States

Location

Yale Univ

New Haven, Connecticut, 06519, United States

Location

Northwestern Univ Med School

Chicago, Illinois, 60611, United States

Location

Indiana Univ Hosp

Indianapolis, Indiana, 462025250, United States

Location

Johns Hopkins Hosp

Baltimore, Maryland, 212052196, United States

Location

Harvard (Massachusetts Gen Hosp)

Boston, Massachusetts, 02114, United States

Location

Boston Med Ctr

Boston, Massachusetts, 02118, United States

Location

Washington Univ

St Louis, Missouri, 63110, United States

Location

Mount Sinai Med Ctr

New York, New York, 10029, United States

Location

North Central Bronx Hosp / Bronx Municipal Hosp

The Bronx, New York, 10467, United States

Location

Univ of North Carolina School of Medicine

Chapel Hill, North Carolina, 275997215, United States

Location

Ohio State Univ Hosp Clinic

Columbus, Ohio, 432101228, United States

Location

Girard Med Ctr

Philadelphia, Pennsylvania, 191046073, United States

Location

Univ TX Galveston Med Branch

Galveston, Texas, 775550882, United States

Location

Univ of Washington / Madison Clinic

Seattle, Washington, 98122, United States

Location

Saint Vincent's Hosp Med Centre

Sydney, Australia

Location

Southern Alberta HIV Clinic / Foothills Hosp

Calgary, Alberta, Canada

Location

Sunnybrook Health Science Ctr

Toronto, Ontario, Canada

Location

Toronto Hosp

Toronto, Ontario, Canada

Location

Montreal Chest Institute

Montreal, Quebec, Canada

Location

Montreal Gen Hosp

Montreal, Quebec, Canada

Location

Hvidovre Univ Hosp

Hvidore, Denmark

Location

Services des Maladies Infectieuses

Paris, France

Location

Universitatsklinikum Rudolf Virchow

Berlin, Germany

Location

Universita Cattolica del Sacro Cuore

Rome, Italy

Location

South Hosp

Stockholm, Sweden

Location

Medizinische Universibatspoliklinik Infekbiologie

Bern, Switzerland

Location

Royal Free Hosp

London, United Kingdom

Location

Westminster Hosp

London, United Kingdom

Location

Related Publications (11)

  • Feinberg JE, Hurwitz S, Cooper D, Sattler FR, MacGregor RR, Powderly W, Holland GN, Griffiths PD, Pollard RB, Youle M, Gill MJ, Holland FJ, Power ME, Owens S, Coakley D, Fry J, Jacobson MA. A randomized, double-blind trial of valaciclovir prophylaxis for cytomegalovirus disease in patients with advanced human immunodeficiency virus infection. AIDS Clinical Trials Group Protocol 204/Glaxo Wellcome 123-014 International CMV Prophylaxis Study Group. J Infect Dis. 1998 Jan;177(1):48-56. doi: 10.1086/513804.

    PMID: 9419169BACKGROUND
  • Fry J, Coakley D, Power M, Feinberg J. International collaborative clinical trials: the ACTG 204 experience. Int Conf AIDS. 1996 Jul 7-12;11(2):276 (abstract no ThB4146)

    BACKGROUND
  • Griffiths PD, Feinberg J. Detection of cytomegalovirus in samples from patients enrolled in ACTG 204 / Glaxo Wellcome 123-014. Conf Retroviruses Opportunistic Infect. 1996 Jan 28-Feb 1;3rd:54

    BACKGROUND
  • Brosgart C, Fisher E, Pulling C, Chaloner K, Cohn D, Elsadr W, Verheggen R, Schmetter B, Alston B. Prevalence of asymptomatic CMV retinitis (CMVR) in AIDS patients. Conf Retroviruses Opportunistic Infect. 1999 Jan 31-Feb 4;6th:152 (abstract no 453)

    BACKGROUND
  • Fisher E, Brosgart C, Cohn D, Chaloner K, Pulling C, Alston B, Schmetter B, El-Sadr W. Placebo (PLC)-controlled, multicenter trial of adefovir dipivoxil (ADV) in patients (pt) with HIV disease. . Conf Retroviruses Opportunistic Infect. 1999 Jan 31-Feb 4;6th:160 (abstract no 491)

    BACKGROUND
  • Feinberg JE, Bell WR, Chulay JD. A thrombotic microangiopathy (TMA)-like syndrome in patients with advanced HIV disease in a cytomegalovirus (CMV) prophylaxis trial (ACTG 204). Conf Retroviruses Opportunistic Infect. 1997 Jan 22-26;4th:196 (abstract no 715)

    BACKGROUND
  • Sprenger HG, Law G, Pastoor G, Postma S, Schirm J, Weits J, The TH. Cytomegalovirus antigenemia (CMVAg) compared with other CMV tests during phase III study of valaciclovir (VACV) for CMV prophylaxis in advanced HIV disease (ACTG 204 study). Int Conf AIDS. 1996 Jul 7-12;11(2):285 (abstract no ThB4200)

    BACKGROUND
  • Bell WR, Chulay JD, Feinberg JE. Manifestations resembling thrombotic microangiopathy in patients with advanced human immunodeficiency virus (HIV) disease in a cytomegalovirus prophylaxis trial (ACTG 204). Medicine (Baltimore). 1997 Sep;76(5):369-80. doi: 10.1097/00005792-199709000-00004. No abstract available.

    PMID: 9352739BACKGROUND
  • Emery V, Sabin C, Feinberg J, Grywacz M, Knight S, Griffiths P. Quantitative effects of valaciclovir on the replication of cytomegalovirus in patients with advanced HIV disease. Conf Retroviruses Opportunistic Infect. 1999 Jan 31-Feb 4;6th:153 (abstract no 459)

    BACKGROUND
  • Weinberg A, Schneider SA, Clark JC. Acyclovir (ACV) and valacyclovir (VAL) prophylaxis of AIDS patients does not alter cytomegalovirus (CMV) susceptibility to ganciclovir (GCV) or foscarnet (FOS). Program Abstr Intersci Conf Antimicrob Agents Chemother. 1996 Sep 15-18:202 (abstract no I87)

    BACKGROUND
  • Nokta MA, Holland F, De Gruttola V, Emery VC, Jacobson MA, Griffiths P, Pollard RB, Feinberg JE; AIDS Clinical Trials Group, Protocol 204/GlaxoWellcome 123-014, International CMV Prophylaxis Study Group. Cytomegalovirus (CMV) polymerase chain reaction profiles in individuals with advanced human immunodeficiency virus infection: relationship to CMV disease. J Infect Dis. 2002 Jun 15;185(12):1717-22. doi: 10.1086/340651. Epub 2002 May 31.

    PMID: 12085316BACKGROUND

MeSH Terms

Conditions

Cytomegalovirus InfectionsHIV InfectionsAcquired Immunodeficiency Syndrome

Interventions

ValacyclovirAcyclovir

Condition Hierarchy (Ancestors)

Herpesviridae InfectionsDNA Virus InfectionsVirus DiseasesInfectionsBlood-Borne InfectionsCommunicable DiseasesSexually Transmitted Diseases, ViralSexually Transmitted DiseasesLentivirus InfectionsRetroviridae InfectionsRNA Virus InfectionsGenital DiseasesUrogenital DiseasesImmunologic Deficiency SyndromesImmune System DiseasesSlow Virus Diseases

Intervention Hierarchy (Ancestors)

GuanineHypoxanthinesPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic Compounds

Study Officials

  • Feinberg J

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
phase 3
Purpose
TREATMENT
Sponsor Type
NIH

Study Record Dates

First Submitted

November 2, 1999

First Posted

August 31, 2001

Primary Completion

May 1, 1996

Last Updated

March 1, 2011

Record last verified: 2011-02

Locations