[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"HIV Vaccine Trials Network\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":74},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100512087","phase-2-evaluating-the-safety-and-immunogenicity-of-mtbvac-100512087",false,"NCT05947890","Evaluating the Safety and Immunogenicity of MTBVAC","A Phase 2a Clinical Trial to Evaluate the Safety and Immunogenicity of MTBVAC","HVTN605A5421","Inclusion Criteria:\n\n* Age of 12 through 55 years, on the day of enrollment.\n* Access to a participating HVTN or ACTG CRS and willingness to be followed for the planned duration of the study.\n* For volunteers 18 years of age or older: ability and willingness to provide informed consent.\n* For volunteers less than 18 years of age: parent or legal guardian is willing and able to provide informed consent for potential participant's study participation; in addition, when applicable per ethics committee policies and procedures, potential participant is willing and able to provide written assent for study participation.\n* Assessment of Understanding (AoU): volunteer demonstrates understanding of this study and completes a questionnaire prior to vaccination with verbal demonstration of understanding of all questionnaire items answered incorrectly.\n* Prior receipt of BCG vaccine in infancy as determined by the site investigator.\n* Agrees not to enroll in another study of an investigational study product until after the last scheduled clinic visit. If a potential participant is already enrolled in another clinical trial, approvals from the other trial sponsor and the HVTN 605\u002FA5421 PSRT are required prior to enrollment into HVTN 605\u002FA5421.\n* Good general health as shown by medical history, physical exam, and screening laboratory tests and assessed by the site investigator.\n* Willingness to receive HIV-related test results.\n* For volunteers living without HIV:\n\n  1. Negative HIV-1 and -2 blood test: Non-US sites may use locally available assays that have been approved by HVTN Laboratory Operations\n  2. Assessed by the clinic staff as having a low likelihood of acquiring HIV and is committed to maintaining behavior that is consistent with a lower likelihood of acquiring HIV through the last required protocol clinic visit\n  3. Willingness to discuss their potential for HIV acquisition and is amenable to HIV risk reduction counseling\n* For volunteers living with HIV:\n\n  1. For both Cohorts 2 and 3: Completed one course of tuberculosis preventive treatment (TPT) as determined by the site investigator.\n\n     Documented HIV viral suppression (Plasma HIV levels \\\u003C 50 copies\u002FmL) collected at least three months and up to 15 months prior to enrollment (with no intervening HIV-1 RNA results ≥ 50 copies\u002FmL) and from screening labs.\n\n     Has been receiving at least 6 months of ART prior to enrollment, as determined by the site investigator\n  2. For Cohort 2: WHO HIV clinical stage 1 or 2 prior to initiation (or re-initiation in case of treatment interruption\u002Fdefault) of ART.\n\nCD4+ T-cell count of ≥ 200 cells\u002Fmm3 (during screening) 3. For Cohort 3: Advanced HIV disease (defined as CD4 count less than 200 cells\u002Fmm3 or WHO HIV clinical stage 3 or 4) prior to initiation (or re-initiation) of ART. Advanced HIV defined as CD4 count less than 200 cells\u002Fmm3 or WHO stage 3 or 4. Current CD4+ T-cell count of ≥ 100 cells\u002F mm3 (during screening)\n\n* Laboratory Inclusion Values - Has normal or Grade 1 results of all of the following at screening:\n\nHemoglobin (≥ 9.5 g\u002FdL or ≥ 5.88 mmol\u002FL for males and females less than 13 years of age; ≥ 9.5 g\u002FdL or ≥ 5.88 mmol\u002FL for females 13 years of age and older; ≥ 10.0 g\u002FdL or ≥ 6.19 mmol\u002FL for males 13 years of age and older); White blood cell count (≥ 2000 cells\u002Fmm3 or ≥ 2.000 × 109 cells\u002FL); Platelet count (≥ 100,000 cells\u002Fmm3 or ≥ 100.000 × 109 cells\u002FL); Creatinine (≤ 1.3 × upper limit of normal \\[ULN\\]); Alanine aminotransferase (ALT) (\\\u003C 2.5 × ULN); Aspartate aminotransferase (AST) (\\\u003C 2.5 × ULN)\n\n* Negative Hepatitis B surface antigen (HBsAg).\n* Negative anti-Hepatitis C virus Abs (anti-HCV), or negative HCV nucleic acid test if the anti-HCV is positive\n* For volunteers assigned female sex at birth (AFAB) or intersex at birth and are of reproductive potential (hereafter referred to as \"of pregnancy potential\"): negative serum or urine beta human chorionic gonadotropin (β-HCG) pregnancy test at screening (ie, prior to randomization) and prior to study product administration on the day of study product administration. Persons who are NOT of pregnancy potential including having reached menopause (no menses for 1 year) or having undergone hysterectomy or bilateral oophorectomy, or tubal ligation (verified by medical records) are not required to undergo pregnancy testing.\n* Reproductive status: A volunteer of pregnancy potential:\n\n  1. Must agree to use effective contraception for sexual activity that could lead to pregnancy from at least 21 days prior to enrollment until 10 weeks after vaccination.\n  2. Volunteers of pregnancy potential must also agree not to seek pregnancy through alternative methods, such as artificial insemination, or in vitro fertilization until 10 weeks after vaccination.\n  3. Volunteers of pregnancy potential must also agree not to undergo oocyte retrieval.\n\nExclusion Criteria:\n\n* Weight less than 40 kg\n* Known significant exposure to TB or receipt of tuberculin skin test in the six months prior enrollment, as determined by the site investigator based on potential participant\u002Fparent\u002Fguardian report and available medical records. \\[Note: Significant exposure is defined as close contact with a person who has active TB and has not completed TB treatment. Close contact is defined as sleeping in the same contiguous house\u002Fdwelling, and\u002For working or socializing in close proximity in an enclosed space frequently (eg, several times a week).\\]\n* History of prior active TB disease, as determined by the site investigator based on participant\u002Fparent\u002Fguardian report and available medical, laboratory or radiographic records.\n* Evidence of active TB disease as determined by the site investigator based on participant\u002Fparent\u002Fguardian report and available medical records, results from physical examination, two-view chest X-ray, and M.tb nucleic acid testing from an expectorated sputum, including a review of any available radiography; and, for volunteers living with HIV and a CD4 count \\\u003C200 cells\u002Fmm3, a positive urine LAM test.\n* Receipt of TB preventive therapy within 28 days prior to enrollment or expected to initiate TB preventive therapy during the study as determined by the site investigator based on participant\u002Fparent\u002Fguardian report and available medical records Note: Clinical indication for receipt of TB preventive therapy will be determined by the site investigator consistent with local standard guidelines. Potential participants on TB preventive therapy during screening may be enrolled once the exclusionary timeframes indicated above have elapsed. If the screening period is exceeded while this requirement is being met, a new screening attempt should be initiated.\n* For volunteers living with HIV: current active AIDS-defining condition as determined by the site investigator based on participant\u002Fparent\u002Fguardian report and available medical records\n* Blood products received within 120 days before vaccination.\n* Investigational study products (non-vaccine) received within 28 days before vaccination.\n* Pregnant or breastfeeding.\n* Investigational TB vaccine(s) received in a prior TB vaccine trial or BCG vaccination outside infancy. For volunteers who have received control\u002Fplacebo in a TB vaccine trial, the HVTN 605\u002FA5421 PSRT will determine eligibility on a case-by-case basis.\n* Investigational non-TB vaccine(s) received within the last 1 year in a prior vaccine trial. Exceptions may be made by the HVTN 605\u002FA5421 PSRT for vaccines that have subsequently undergone licensure by the FDA or by the national regulatory authority where the volunteer is enrolling. For volunteers who have received control\u002Fplacebo in an experimental vaccine trial, the HVTN 605\u002FA5421 PSRT will determine eligibility on a case-by-case basis. For volunteers who have received an experimental vaccine(s) greater than 1 years ago, eligibility for enrollment will be determined by the HVTN 605\u002FA5421 PSRT on a case-by-case basis.\n* Live attenuated vaccines received within 28 days before first vaccination or scheduled within 28 days after injection (eg, measles, mumps, and rubella \\[MMR\\]; oral polio vaccine \\[OPV\\]; varicella; yellow fever; live attenuated influenza vaccine).\n* Any vaccines that are not live attenuated vaccines and were received within 14 days prior to first vaccination (eg, tetanus, pneumococcal, Hepatitis A or B).\n* Allergy treatment with antigen injections within 28 days before first vaccination or that are scheduled within 14 days after first vaccination.\n* Immunosuppressive medications received within 168 days before first vaccination (Not exclusionary: \\[1\\] corticosteroid nasal spray; \\[2\\] inhaled corticosteroids; \\[3\\] topical corticosteroids for mild, uncomplicated dermatologic condition; or \\[4\\] a single course of oral\u002Fparenteral prednisone or equivalent at doses \\\u003C 60 mg\u002Fday and length of therapy \\\u003C 11 days with completion at least 30 days prior to enrollment).\n* Serious adverse reactions to vaccines or to vaccine components including history of anaphylaxis and related symptoms such as hives, respiratory difficulty, angioedema, and\u002For abdominal pain. (Not excluded from participation: a volunteer who had a non-anaphylactic adverse reaction to pertussis vaccine as a child).\n* Immunoglobulin received within 90 days before vaccination.\n* Autoimmune disease, current or history (Not exclusionary: mild, well-controlled psoriasis)\n* Immunodeficiency (Not exclusionary: HIV).\n* Clinically significant medical condition, physical examination findings, clinically significant abnormal laboratory results, or past medical history with clinically significant implications for current health. A clinically significant condition or process includes but is not limited to:\n\n  1. A process that would affect the immune response,\n  2. A process that would require medication that affects the immune response,\n  3. Any contraindication to repeated injections or blood draws,\n  4. A condition that requires active medical intervention or monitoring to avert grave danger to the volunteer's health or well-being during the study period,\n  5. A condition or process for which signs or symptoms could be confused with reactions to vaccine, or\n  6. Any condition specifically listed among the exclusion criteria below.\n* Any medical, psychiatric, occupational, or other condition that, in the judgment of the investigator, would interfere with, or serve as a contraindication to, protocol adherence, assessment of safety or reactogenicity, or a volunteer's ability to give informed consent, including but not limited to clinically significant substance or alcohol use disorder.\n* Psychiatric condition that precludes compliance with the protocol. Specifically excluded are persons with psychoses within the past 3 years, ongoing risk for suicide, or history of suicide attempt or gesture within the past 3 years.\n* Asthma exclusion criteria:\n\nAsthma is exclusionary if the participant has ANY of the following:\n\n1\\. Required either oral or parenteral corticosteroids for an exacerbation 2 or more times within the past year; OR 2. Needed emergency care, urgent care, hospitalization, or intubation for an acute asthma exacerbation within the past year (eg, would NOT exclude individuals with asthma who meet all other criteria but sought urgent\u002Femergent care solely for asthma medication refills or coexisting conditions unrelated to asthma); OR 3. Uses a short-acting rescue inhaler more than 2 days\u002Fweek for acute asthma symptoms (ie, not for preventive treatment prior to athletic activity); OR 4. Uses medium-to-high-dose inhaled corticosteroids (greater than 250 mcg fluticasone or therapeutic equivalent per day), whether in single-therapy or dual-therapy inhalers (ie, with a long-acting beta agonist \\[LABA\\]); OR Uses more than 1 medication for maintenance therapy daily. Inclusion of anyone on a stable dose of more than 1 medication for maintenance therapy daily for greater than 2 years requires PSRT approval.\n\n* Diabetes mellitus type 1 or type 2. (Not exclusionary: type 2 cases controlled with diet alone or a history of isolated gestational diabetes. For these cases, control should be confirmed with an appropriate laboratory test (eg, fasting glucose, HbA1c) based on a specimen collected during screening.)\n* Hypertension:\n\n  1. If a person has been found to have elevated blood pressure or hypertension during screening or previously, exclude for blood pressure that is not well controlled. Well-controlled blood pressure is defined in this protocol as consistently \\\u003C 140 mm Hg systolic and \\\u003C 90 mm Hg diastolic, with or without medication, with only isolated, brief instances of higher readings, which must be ≤ 150 mm Hg systolic and ≤ 100 mm Hg diastolic. For these volunteers, blood pressure must be \\\u003C 140 mm Hg systolic and \\\u003C 90 mm Hg diastolic at enrollment.\n  2. If a person has NOT been found to have elevated blood pressure or hypertension during screening or previously, exclude for systolic blood pressure ≥ 150 mm Hg at enrollment or diastolic blood pressure ≥ 100 mm Hg at enrollment.\n* Bleeding disorder (eg, factor deficiency, coagulopathy, or platelet disorder requiring special precautions)\n* Malignancy (Not excluded from participation: Volunteer who has had malignancy excised surgically and who, in the investigator's estimation, has a reasonable assurance of sustained cure, or who is unlikely to experience recurrence of malignancy during the period of the study).\n* Seizure disorder: History of seizure(s) within past three years. Also exclude if volunteer has used medications in order to prevent or treat seizure(s) at any time within the past 3 years.\n* Asplenia: any condition resulting in the absence of a functional spleen.\n* History of angioedema or anaphylaxis (Not exclusionary: angioedema or anaphylaxis with known trigger and no episodes within five years.)\n* History of generalized urticaria within past five years.",true,"ALL","12 Years","55 Years",{"count":22,"type":23},276,"ESTIMATED","INTERVENTIONAL",[26],"PHASE2","The purpose of this study is to evaluate the safety and immunogenicity of MTBVAC in adolescents and adults living with and without HIV in South Africa",[29,30],"HIV I Infection","Tuberculosis",[32,33],"HIV","TB","RECRUITING","2026-03-10",{"date":37,"type":38},"2026-03-12","ACTUAL",{"date":40,"type":38},"2024-01-30",{"date":42,"type":23},"2027-04-05",{"name":44,"class":45},"HIV Vaccine Trials Network","NETWORK",16,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":24,"phases":58,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},"100563255","phase-1-safety--immunogenicity-of-426cmodcore-c4b-vaccine-with-3m-052-afalum-in-infants-perinatally-exposed-to-hiv-but-uninfected-100563255","NCT06613789","Safety & Immunogenicity of 426c.Mod.Core-C4b Vaccine With 3M-052-AF+Alum in Infants Perinatally Exposed to HIV But Uninfected","A Partially Randomized Phase 1 Clinical Trial to Evaluate the Safety and Immunogenicity of 426c.Mod.Core-C4b Vaccine Adjuvanted With 3M-052-AF + Alum in Infants With Perinatal HIV Exposure Who Are Without HIV at Birth","HVTN316","Inclusion Criteria: Mother\n\n* Mother's age is at least 18 years and is willing and able to provide written informed consent for their and their infant's participation in this study\n* Mother is in the second or third trimester of singleton pregnancy, as determined by a clinical exam or sonography and reported menstrual history\n* Mother agrees to donate umbilical cord blood\n* Mother has a planned Caesarian delivery at Chris Hani Baragwanath Academic Hospital (Soweto) and plans to remain in the area after delivery and through study duration\n* Mother is determined by the site investigator to be in good overall health at the time of delivery based on medical history and physical exam\n* Mother has a documented CD4 count of more than 350 cells\u002FmcL at screening\n* Mother has been on cART for at least 16 weeks prior to delivery and intends to continue with cART for the duration of breastfeeding\n* Mother has a viral load of less than 400 copies\u002FmL between 2 weeks before and 7 days after delivery\n* Mother has access to the participating HVTN CRS and is willing to be followed for the planned duration of the study\n* Mother demonstrates understanding of this study and is able and willing to complete the informed consent process and delivery with verbal demonstration of understanding of all questionnaire items answered incorrectly\n* Mother agrees not to enroll either self or infant in another research study for the duration of the trial without prior approval of the HVTN 316 PSRT.\n* Mother has confirmed positive HIV-1 status documented by medical records at any time during or prior to screening, and confirmed by the HVTN CRS by serology\n\nExclusion Criteria: Mother\n\n* Any World Health Organization (WHO) grade IV illness within 1 year prior to study enrollment, as determined by the history and physical examination and review of the medical record (if available). These include HIV wasting syndrome; PJP pneumonia; cerebral toxoplasmosis; extrapulmonary cryptococcosis; progressive multifocal leukoencephalopathy; any disseminated endemic mycosis (histoplasmosis); candidiasis of the esophagus, trachea, bronchi, or lung; disseminated atypical mycobacteria; non-typhoid salmonella septicemia; extrapulmonary tuberculosis; lymphoma; and Kaposi's sarcoma.\n* Prior participation in any HIV-1 vaccine or anti-HIV antibody-mediated prevention trial\n* Receipt of any investigational agent during this pregnancy\n* Receipt of blood products, immunoglobulin (Ig), or immunomodulating therapy within 45 days prior to, and the day of delivery\n* Any medical, psychiatric, occupational, or other condition that, in the judgment of the investigator, would interfere with or serve as a contraindication to protocol adherence, assessment of infant safety or reactogenicity, or a volunteer's ability to give informed consent\n* Any condition that places the newborn at higher risk of early-onset sepsis, such as concern for active maternal infection at delivery, as determined by local site investigators (eg, fever)\n* Detectable hepatitis B surface antigen (HBsAg)\n\nInclusion Criteria: Infant\n\n* Born via Caesarean delivery to a pregnant woman living with HIV-1 who meets all maternal inclusion\u002Fexclusion criteria listed above\n* Estimated gestational age at birth is at least 37 weeks\n\nNote: If gestational age at birth is not documented in the infant's available birth records, study staff may assess gestational age at the earliest possible opportunity during the screening period and use this assessment for purposes of eligibility determination.\n\n* Weight at birth is at least 2.5 kg\n* Has initiated ARV prophylaxis consistent with current site-specific standard of care\n* Hemoglobin (HgB) more than 14.0 g\u002FdL\n* White blood cell (WBC) count ≥ 7,000 cells\u002Fmm3\n* Platelets more than 100,000 cells\u002Fmm3\n* Alanine aminotransferase (ALT) less than 1.25 times upper limit of age-adjusted normal\n* Creatinine less than 1.1 times upper limit of age adjusted normal\n* Negative HIV-1 nucleic acid test (NAT) on specimen drawn within 72 hours of birth\n* Written informed consent provided by mother\n* Age is equal to or less than 7 days\n\nExclusion Criteria: Infant\n\n* Any clinically significant congenital anomaly\u002Fbirth defect\n* Documented or suspected serious medical illness, infection, clinically significant finding from physical examination, or immediate life-threatening condition, including requirement for ongoing supplemental oxygen, as judged by the examining clinician\n* Receipt of or anticipated need for blood products, immunoglobulin, or immunosuppressive therapy. This includes infants who require hepatitis B immunoglobulin (HBIG), but it does not require exclusion of infants who receive hepatitis B vaccine in the newborn period.\n* Receipt of any other investigational product","7 Days",{"count":57,"type":23},22,[59],"PHASE1","The purpose of this study is to evaluate the safety and immunogenicity of 426c.Mod.Core-C4b vaccine adjuvanted with 3M-052-AF + Alum in infants with perinatal HIV exposure who are without HIV at birth",[62],"HIV Infections",[32],"NOT_YET_RECRUITING","2025-12-05",{"date":67,"type":38},"2025-12-09",{"date":69,"type":23},"2026-07-13",{"date":71,"type":23},"2027-06-03",{"name":44,"class":45},1,""]