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Enrollment Closed

Home/Clinical trials/Enrollment Closed
Enrollment Closedjsukhram2020-05-19T19:10:26+00:00
#CategoryStatusStudy
1HIVEnrollment ClosedMK8591A-018
A Phase 3, Randomized, Active-Controlled, Double-Blind Clinical Study to Evaluate a Switch to MK-8591A Once-Daily in Participants with HIV-1 Virologically Suppressed on Biktarvy

Major Inclusion/Exclusion Criteria:

  1. Currently on Biktarvy for at least 3 months
  2. HIV RNA <50 while on Biktarvy
  3. CD4 >100

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2HIVEnrollment ClosedMK8591A-017
A Phase 3 Randomized, Active-Controlled, Open-Label Clinical Study to Evaluate a Switch to MK-8591A Once-Daily in participants with HIV-1 Virologically Suppressed on Antiretroviral Therapy (ART).

Major Inclusion/Exclusion Criteria:

  1. <50 HIV RNA for greater than 3 months
  2. CD4 >100
  3. GFR >30
  4. No resistance to Doravarine

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3HIVEnrollment ClosedMK1439-018
A Phase 3 Multicenter, Double-Blind, Randomized, Active Comparator-Controlled Clinical Trial to Evaluate the Safety and Efficacy of Doravirine (MK-1439) 100 mg Once Daily Versus Darunavir 800 mg Once Daily Plus Ritonavir 100 mg Once Daily, Each in Combination With TRUVADA™ or EPZICOM™/KIVEXA™, in Treatment-Naïve HIV-1 Infected Subjects

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4HIVEnrollment ClosedGS-US-292-1825
Safety, Tolerability, Pharmacokinetics, and Efficacy of E/C/F/TAF Fixed Dose Combination (FDC) in HIV-1 Infected Adults on Chronic Hemodialysis

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5HIVEnrollment ClosedGS-US-292-1824
Switching to Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (E/C/F/TAF) Fixed Dose Combination (FDC) in Virologically-Suppressed HIV-1 Infected Adults Harboring the Archived Isolated NRTI Resistance Mutation M184V/M184I

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6HIVEnrollment ClosedGS-US-382-3961
Evaluate the Safety and Efficacy of Vesatolimod in Antiretroviral Treated HIV-1 Infected Controllers

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7HIVEnrollment ClosedFrontier ABT-3BNC117201
Albuvirtide and 3BNC117 as Long-Acting Maintenance Therapy in Virologically Suppressed Subjects (ABL)

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8HIVEnrollment ClosedViiV 200056
A Phase IIb Study to Evaluate a Long-Acting Intramuscular Regimen for Maintenance of Virologic Suppression (Following Induction With an Oral Regimen of GSK1265744 and Abacavir/Lamivudine) in Human Immunodeficiency Virus Type 1 (HIV-1) Infected, Antiretroviral Therapy-Naive Adult Subjects

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9HIVEnrollment ClosedViiV AI438-047/205888
Attachment Inhibitor Comparison in Heavily Treatment Experienced Patients

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10HIVEnrollment ClosedJanssen TMC114IFD3013
Study to Evaluate Efficacy and Safety of Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (D/C/F/TAF) Regimen Versus Boosted Protease Inhibitor (bPI) Along With Emtricitabine/Tenofovir Disoproxil Fumarate (FTC/TDF) Regimen in Virologically-Suppressed, HIV-1 Infected Participants

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11HIVEnrollment ClosedJanssen TMC114FD2HTX3001
A Study to Evaluate Efficacy and Safety of Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (D/C/F/TAF) Fixed Dose Combination (FDC) Versus a Regimen Consisting of Darunavir/Cobicistat FDC With Emtricitabine/Tenofovir Disoproxil Fumarate FDC in Treatment-naive HIV Type 1 Infected Subjects

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12HIVEnrollment ClosedGS-US-380-1490
Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Dolutegravir + Emtricitabine/Tenofovir Alafenamide in HIV-1 Infected, Antiretroviral Treatment-Naive Adults

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13HIVEnrollment ClosedGS-US-380-1489
Safety and Efficacy of Bictegravir/Emtricitabine/Tenofovir Alafenamide Versus Abacavir/Dolutegravir/Lamivudine in HIV-1 Infected, Antiretroviral Treatment-Naïve Adults

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14HIVEnrollment ClosedViiV 205543
An Efficacy, Safety, and Tolerability Study Comparing Dolutegravir (DTG) Plus Lamivudine (3TC) With Dolutegravir Plus Tenofovir/Emtricitabine in Treatment naïve HIV Infected Subjects (Gemini 2)

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15HIVEnrollment ClosedViiV 204861
An Efficacy, Safety, and Tolerability Study Comparing Dolutegravir Plus Lamivudine With Dolutegravir Plus Tenofovir/Emtricitabine in Treatment naïve HIV Infected Subjects (Gemini 1)

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16HIVEnrollment ClosedViiV 201585
Study Evaluating the Efficacy, Safety, and Tolerability of Switching to Long-acting Cabotegravir Plus Long-acting Rilpivirine From Current Antiretroviral Regimen in Virologically Suppressed HIV-1-infected Adults

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17HIVEnrollment ClosedCytoDyn PRO140_CD03
Study of PRO 140 SC as Single Agent Maintenance Therapy in Virally Suppressed Subjects With CCR5-tropic HIV-1 Infection

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18HIVEnrollment ClosedGS-US-380-1474
B/F/TAF FDC in HIV-1 Infected Virologically Suppressed Adolescents and Children

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19HIVEnrollment ClosedGS-US-380-4030
Switching to a Fixed Dose Combination of Bictegravir/Emtricitabine/Tenofovir Alafenamide (B/F/TAF) in HIV-1 Infected Adults Who Are Virologically Suppressed

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20HIVEnrollment ClosedViiV 204862
Switch Study to Evaluate Dolutegravir Plus Lamivudine in Virologically Suppressed Human Immunodeficiency Virus Type 1 Positive Adults (TANGO)

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21HIVEnrollment ClosedViiV 207966
Efficacy, Safety and Tolerability Study of Long-acting Cabotegravir Plus Long-acting Rilpivirine (CAB LA + RPV LA) in Human-immunodeficiency Virus-1 (HIV-1) Infected Adults

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22HIVEnrollment ClosedViiV 209035
Phase 2b, Open-label, Multicenter, Rollover Study to Assess Antiviral Activity and Safety of Long-acting Cabotegravir (CAB LA) Plus Long-acting Rilpivirine (RPV LA), Administered Every 2 Months (Q2M), in Human Immunodeficiency Virus (HIV)- Positive Subjects From the LATTE Study

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23HIVEnrollment ClosedGS-US-380-4580
Switching From a Regimen of Two Nucleos(t)Ide Reverse Transcriptase Inhibitors (NRTI) Plus a Third Agent to a Fixed Dose Combination (FDC) of Bictegravir/Emtricitabine/Tenofovir Alafenamide (B/F/TAF), in Virologically-Suppressed, HIV-1 Infected African American Participants

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24HIVEnrollment Closed212355 (STAT)
Rapid Test and Treat Dolutegravir Plus Lamivudine Study in Newly Diagnosed Human Immunodeficiency Virus (HIV)-1 Infected Adults

Major Inclusion/Exclusion Criteria:

  1. HIV Treatment Naive 
  2. Diagnosed within 14 days prior to Screening
  3. No Hepatitis B infection

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25HIVEnrollment ClosedGS-US-200-4072Opened 11/14/2018
Safety, Pharmacokinetics, and Antiviral Activity of GS-6207 Administered Subcutaneously in HIV-1 Infected Adults

Major Inclusion/Exclusion Criteria

    1. Never have taken HIV medications or have been off HIV medications more than 12 weeks
    2. No history of taking integrase inhibitor HIV medication
    3. Absolute CD4 > 200
    4. Willing to start Biktarvy on day 10 of the clinical trial
    5. No medications taken within 42 days prior to start of the study drug without prior approval from Sponsor

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26OtherEnrollment ClosedGS-US-412-2055
Safety and Efficacy of Emtricitabine and Tenofovir Alafenamide (F/TAF) Fixed-Dose Combination Once Daily for Pre-Exposure Prophylaxis in Men and Transgender Women Who Have Sex With Men and Are At Risk of HIV-1 Infection (DISCOVER)

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