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Study of Combinations of Novel Promising Drugs for Pulmonary Tuberculosis (SYNERGY)

14 agosto 2026 aggiornato da: TASK Applied Science

A Phase 2, Randomised, Controlled, Multicentre Two-Part Trial Assessing the Safety and Efficacy of TBAJ-587 as Part of a Combination Regimen in Newly Diagnosed, Drug-Sensitive, Sputum-Positive Pulmonary Tuberculosis

A phase 2, two-part, multicentre, open label, controlled, randomised clinical trial in adult participants with newly diagnosed, sputum-positive pulmonary drug-sensitive tuberculosis (DSTB). Assessing the Safety and Efficacy of TBAJ-587 as Part of a Combination Regimen in Newly Diagnosed, Drug-Sensitive, Sputum-Positive Pulmonary Tuberculosis

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

This is a phase 2, two-part, multicentre, open label, controlled, randomised clinical trial in adult participants with newly diagnosed, sputum-positive pulmonary DS-TB. The trial will be performed in two sequential parts, each part containing parallel treatment arms.

Part A: Participants will be randomly assigned to one of two TBAJ-587 experimental regimens (TBA-587PaL, 100 mg or 200mg dose) or the active SOC control arm (HRZE:). Data from Part A will inform dose selection for Part B.

Part B: Participants will be randomly assigned to one of three experimental regimens. The sequential design allows for an interim analysis (section 10.5) between Parts A and B to evaluate the safety and efficacy of lower and higher TBAJ-587 doses before progressing to Part B, where the selected dose will be used. TBAJ-587 may be replaced by a similar diarylquinolone compound if, based on the interim analysis - for scientific and/or safety reasons - determines that TBAJ-587 should not proceed into Part B. Should this occur, the protocol will be updated via submission of a formal protocol amendment.

The active control arm included in Part A provides an internal benchmark to confirm that study procedures, microbiological methods, and clinical conduct perform as expected. Data generated from the Part A control arm will therefore serve as the primary internal reference for interpretation of Part B results. Therefore, there is no control arm in Part B.

In addition, the bacteriological endpoints used in this study, including time to positivity (TTP) and related measures of early bactericidal activity, are well characterised for HRZE in the published literature. These established external data provide a robust contextual framework against which Part B outcomes can be interpreted, without the need for an additional concurrent control arm.

This approach limits unnecessary exposure of participants to standard therapy beyond what is required to establish study validity, while allowing efficient evaluation of the selected investigational regimen in Part B.

Tipo di studio

Interventistico

Iscrizione (Stimato)

135

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Western Cape
      • Cape Town, Western Cape, Sud Africa, 7405

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • To be eligible to participate in this trial, an individual must meet all the following criteria:

    1. Provide written informed consent.
    2. Male or female aged 18-65 (inclusive)
    3. Clinical evidence of active TB disease, meeting either or both of the following criteria:

      1. Symptoms consistent with pulmonary TB at screening AND/OR
      2. Imaging findings consistent with active pulmonary TB on chest X-ray performed at screening or within 15 days prior to screening.
    4. At least one sputum specimen produced at screening tested on either of the following:

      Xpert MTB/XDR and Ultra with:

      • positive for M. tb
      • a semi-quantitative result of 'medium' (cycle threshold value of >16-22) or 'high' (cycle threshold value of >16-22) AND
      • does not show rifampicin and/or isoniazid resistance. OR

        a. Sputum smear

      • Sputum positive for tubercle bacilli (at least 1+ on the IUATLD/WHO scale on smear microscopy) AND o Sensitive to rifampicin and isoniazid by rapid sputum-based test.
    5. Able to produce a spot sputum with a volume of at least 4 ml.
    6. Body weight within the range of 30 to 100 kgs and body mass index within the range of 15 to 40 kg/m2.
    7. Newly diagnosed and untreated for this episode of TB.
    8. Individuals with a history of TB may be enrolled in this trial if they meet the following criteria:

      1. had a good treatment response in the opinion of the investigator (previous TB symptoms improved sufficiently or resolved) AND
      2. completed their previous TB treatment AND
      3. received their last dose of treatment more than 6 months before trial treatment AND • remained clinically well after completing treatment for their previous TB.
    9. Willing to abstain from alcohol and tyramine containing foods for the treatment duration.
    10. Willing to comply with study visits, all study procedures and treatment observation.

Exclusion Criteria:

  • An individual who meets any of the following criteria will be excluded from participation in this trial:

    1. Taken more than 1 daily dose of medication with anti-tuberculous activity during the 14 days prior to randomisation (isoniazid, rifampicin, pyrazinamide, ethambutol, linezolid, moxifloxacin, levofloxacin or amikacin).
    2. Known or suspected extra-thoracic TB, miliary TB or disseminated TB (in the judgement of the investigator; note uncomplicated pleural effusion occupying <50% of hemithorax or concomitant intra- or extra-thoracic lymphadenopathy are not exclusions).
    3. Severe clinical pulmonary TB e.g. respiratory failure or complications, likely to require hospital admission in the opinion of the investigator.
    4. Poor general condition (Karnofsky score ≤50) OR where any delay in treatment cannot be tolerated in the opinion of the investigator.
    5. Active malignancy requiring systemic therapy, radiotherapy or palliative therapy.
    6. History of myocardial infarction, coronary heart disease or congestive cardiac failure; long QT syndrome or clinically significant arrhythmias; pulmonary hypertension; any known congenital cardiac problems; family history of long QT syndrome or sudden death from unknown or cardiac related cause; uncontrolled arterial hypertension (not excluded if this is corrected prior to randomisation).
    7. Cardiac valve abnormalities identified on echocardiogram.
    8. History of vitiligo.
    9. History of, or ongoing, inflammatory skin disorder such as leprosy, eczema, psoriasis, lichen planus, or other skin rash that would, in the opinion of the investigator, compromise the participant's safety or outcome in the trial.
    10. History of seizure(s).
    11. History of vascular aneurysm.
    12. Symptomatic peripheral neuropathy causing greater than minimal interference with usual social and functional activities.
    13. History of optic neuritis.
    14. Current alcohol or illicit drug use sufficient to compromise the safety of the participant or research staff or compromise adherence to study procedures, in the opinion of the investigator.
    15. Any current or recent use of amphetamines or methamphetamines evident on toxicity screen.
    16. Any other medically or socially significant condition (e.g. psychiatric illness, chronic diarrhoeal disease, metabolic condition, other cardiovascular disease not listed under criterion 6), that would, in the opinion of the investigator, compromise the participant's safety or outcome in the trial; or lead to poor compliance with study visits and protocol requirements; or compromise the interpretation of trial safety and efficacy endpoints.
    17. Women who are currently pregnant or breast-feeding.
    18. Women of childbearing potential (WOCBP) who have had sexual intercourse without contraception after last menses or within the last 3 weeks (whichever is later); or, if unwilling to disclose this information, unable to provide two negative pregnancy tests 8 days apart during the screening period and on day 1 prior to randomisation .
    19. WOCBP unwilling or unable to use appropriate non-user dependent contraception during the study intervention period and for at least 6 months after the last dose of study intervention; and unwilling to commit to refrain from donating eggs (ova, oocytes) for the purpose of reproduction during this period
    20. Men who are unwilling to use a condom during the study period and for at least 90 days after the last dose of study drug to prevent pregnancy, unless they have had a vasectomy; and are unwilling to commit to refrain from donating fresh unwashed semen.
    21. Known allergy to one or more of the study drugs.
    22. Taking a concomitant medication that has a known or predicted interaction with any of the study drugs to which the participant might be randomised

      The participant need not be excluded if:

      1. the concomitant medication can be stopped or replaced with an alternative non-interacting medication, if needed AND
      2. the investigator judges there to be no residual clinical risk to the participant after stopping the concomitant medication (taking into account the washout period of 5x the half-life of the concomitant medication and the duration of the effect of the interaction on levels of study medication).
    23. Taking a concomitant medication that is known to prolong the QTc interval. The participant need not be excluded if the concomitant medication can be stopped or replaced with an alternative medication, if needed, and the duration of the QTc prolongation is expected to resolve prior to dosing of study medication (taking into account the washout period of 5x the half-life of the concomitant medication).
    24. Treatment with any immunosuppressive drugs within the 2 weeks prior to screening (taking systemic corticosteroids for less than 5 consecutive days and stopped at or prior to screening is not an exclusion; topical or inhaled steroids that are taken at a dose below the threshold considered to have systemic immunosuppressive effects are not excluded).
    25. Participation in other clinical intervention trials with an investigational agent within 8 weeks prior to the first dosing day in this trial.
    26. 12-lead ECGs at screening or at baseline shows QTcF >450 ms (men) or >460 ms (women) calculated by Fridericia's formula; and/or any other clinically significant abnormality such as arrhythmia or ischaemia.
    27. Any of the following laboratory parameters at screening:

      1. Hemoglobin < 9 g/dl
      2. Platelet count < 100 x 109 cells/L
      3. Absolute neutrophil count <1 000 cells/μL
      4. eGFR <75 ml/min, calculated using race free CKD EPI 2021 eGFR normalised by body surface area through additional inclusion of weight AND height parameters (not excluded if corrected to above this level)
      5. Alanine Aminotransferase (ALT) or Aspartate Aminotransferase (AST) > 3 times the upper limit of normal (ULN)
      6. Total bilirubin > 1.5 times the ULN
      7. Serum potassium <3.5 mmol/L (not excluded if corrected to above this level)
      8. Serum magnesium < 0.50mmol/L (not excluded if corrected to above this level)
      9. Serum calcium (corrected for albumin level) < 2.10 mmol/L (not excluded if corrected to above this level).
      10. HbA1C >8.0%
    28. Hepatitis B surface antigen positive (known, or on a test performed at screening), hepatitis A IgM and hepatitis C antibodies. (Participants with positive hepatitis C antibodies but negative PCR can be allowed in the trial)
    29. Human Immunodeficiency Virus (HIV) antibody positive (known, or on test performed at screening) unless ALL of the following conditions are met:

      1. Viral load (HIV-RNA) below 200 copies/mL on the last test, done within the previous 90 days (or at screening if no test performed in the previous 90 days).
      2. CD4 count > 200 cells/mm3 on the last test, done within the previous 90 days (or at screening if no test performed in the previous 90 days).
      3. The participant has been taking a regimen of dolutegravir (DTG), tenofovir (TFV) and lamivudine(3TC)/emtricitabine for at least 6 months prior to screening with good adherence.
    30. For Part B only: Participants unwilling or unable to disclose information regarding their last unprotected sexual intercourse (UPSI), or whose responses are considered unreliable or non-compliant by the Investigator.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Arm 1
TBAJ-587 100 mg OD plus Pa 200 mg OD plus L 600 mg OD for 8 weeks
TBAJ-587LD Tablet 50 mg 100 mg OD TBAJ-587HD Tablet 50 mg 200 mg OD TBAJ-587SD Tablet 50 mg Dose selected from Part A daily
Altri nomi:
  • Pretomanid 200mg and Linezolid 600mg
Pretomanid Tablet 200 mg 200 mg OD
600 mg OD
Sperimentale: Arm 2
TBAJ-587 200 mg OD plus Pa 200 mg OD plus L 600 mg OD for 8 weeks
TBAJ-587LD Tablet 50 mg 100 mg OD TBAJ-587HD Tablet 50 mg 200 mg OD TBAJ-587SD Tablet 50 mg Dose selected from Part A daily
Altri nomi:
  • Pretomanid 200mg and Linezolid 600mg
Pretomanid Tablet 200 mg 200 mg OD
600 mg OD
Comparatore attivo: Arm 3
H 75 mg, R 150 mg, Z 400 mg, E 275 mg fixed dose combination, weight-based dosing for 8 weeks
H 75 mg, R 150 mg, Z 400 mg, E 275 mg fixed dose combination
Sperimentale: Arm 4
TBAJ-587 selected dose OD plus Pa 200 mg OD plus T 1 000 mg OD for 8 weeks
TBAJ-587LD Tablet 50 mg 100 mg OD TBAJ-587HD Tablet 50 mg 200 mg OD TBAJ-587SD Tablet 50 mg Dose selected from Part A daily
Altri nomi:
  • Pretomanid 200mg and Linezolid 600mg
Pretomanid Tablet 200 mg 200 mg OD
1 000 mg OD
Sperimentale: Arm 5
TBAJ-587 selected dose OD plus Pa 200 mg OD plus Q 30 mg OD for 8 weeks
TBAJ-587LD Tablet 50 mg 100 mg OD TBAJ-587HD Tablet 50 mg 200 mg OD TBAJ-587SD Tablet 50 mg Dose selected from Part A daily
Altri nomi:
  • Pretomanid 200mg and Linezolid 600mg
Pretomanid Tablet 200 mg 200 mg OD
30 mg OD
Sperimentale: Arm 6
TBAJ-587 selected dose OD plus Pa 200 mg OD plus G 20 mg OD plus L 600 mg OD for 8 weeks
TBAJ-587LD Tablet 50 mg 100 mg OD TBAJ-587HD Tablet 50 mg 200 mg OD TBAJ-587SD Tablet 50 mg Dose selected from Part A daily
Altri nomi:
  • Pretomanid 200mg and Linezolid 600mg
Pretomanid Tablet 200 mg 200 mg OD
600 mg OD
20 mg OD

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Rate of Change in Log10-Transformed Sputum Culture Time to Positivity From Baseline Through Week 8
Lasso di tempo: From baseline to the end of treatment at 8 weeks
Time to positivity is the time, measured in hours, required for a sputum culture to produce a positive result indicating detectable growth of Mycobacterium tuberculosis. The rate of change in log10-transformed time to positivity will be estimated for each treatment arm. Increasing time to positivity indicates a reduction in the viable mycobacterial load in sputum. Measured as change in log10(days).
From baseline to the end of treatment at 8 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Time to Sustained Sputum Culture Conversion From Baseline Through Week 8
Lasso di tempo: From baseline to the end of treatment at 8 weeks
Sustained sputum culture conversion is defined as the first of two consecutive negative sputum cultures, with no subsequent positive culture. Time to conversion will be calculated from baseline to the date of the first negative culture that meets this definition. Measured in days.
From baseline to the end of treatment at 8 weeks
Percentage of Participants With Sustained Sputum Culture Conversion at Week 8
Lasso di tempo: At the end of treatment at 8 weeks
Sustained sputum culture conversion is defined as the first of two consecutive negative sputum cultures, with no subsequent positive culture. Participants who meet this definition by Week 8 will be included in the percentage. Measured as percentage of participants.
At the end of treatment at 8 weeks
Percentage of Participants With Treatment-Emergent Adverse Events
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
A treatment-emergent adverse event (TEAE) is an adverse event that begins or worsens after the participant receives the first dose of study treatment. Participants experiencing one or more TEAEs will be counted once. Measured as percentage of participants.
From enrollment through the final follow-up visit at Week 12
Percentage of Participants With Treatment-Emergent Adverse Events by Maximum Severity Grade as Assessed by CTCAE Version 5.0
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
The severity of each TEAE will be graded using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Grades range from 1 to 5: Grade 1 is mild, Grade 2 is moderate, Grade 3 is severe, Grade 4 is life-threatening and Grade 5 is death. Participants will be summarized according to their maximum recorded severity grade. Measured as percentage of participants.
From enrollment through the final follow-up visit at Week 12
Percentage of Participants With Drug-Related Treatment-Emergent Adverse Events
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
A drug-related TEAE is a treatment-emergent adverse event assessed by the investigator as having a causal relationship to one or more study drugs. Participants experiencing one or more drug-related TEAEs will be counted once. Measured as percentage of participants.
From enrollment through the final follow-up visit at Week 12
Percentage of Participants With Serious Treatment-Emerent Adverse Events
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
A serious TEAE is a treatment-emergent adverse event that results in death, is life-threatening, requires or prolongs inpatient hospitalization, results in persistent or significant disability or incapacity, causes a congenital anomaly or birth defect, or is considered another medically important event. Participants experiencing one or more serious TEAEs will be counted once. Measured as percentage of participants.
From enrollment through the final follow-up visit at Week 12
Percentage of Participants With Treatment-Emergent Adverse Events Leading to Treatment Discontinuation
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
Participants who permanently discontinue one or more study drugs because of a TEAE will be included in this measure. Participants experiencing more than one qualifying event will be counted once. Measured as a percentage of participants.
From enrollment through the final follow-up visit at Week 12
Percentage of Participants With Treatment-Emergent Adverse Events Leading to Death
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
Participants who die as a result of a TEAE will be included in this measure. Each participant will be counted once, regardless of the number of TEAEs contributing to the death. Measured as a percentage of participants.
From enrollment through the final follow-up visit at Week 12
Percentage of Participants With Adverse Events of Special Interest
Lasso di tempo: From enrollment through the final follow-up visit at Week 12
Adverse events of special interest are protocol-defined events that require specific monitoring because of their potential clinical importance in relation to the study drugs. Participants experiencing one or more adverse events of special interest will be counted once. Measured as a percentage of participants.
From enrollment through the final follow-up visit at Week 12
Maximum Observed Plasma Concentration of Study Drugs and Their Metabolites
Lasso di tempo: At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
The maximum observed plasma concentration (Cmax) will be estimated using non-compartmental analysis for the applicable study drugs and metabolites in each treatment arm. These include TBAJ-587 and its metabolites M2, M3 and M12; pretomanid; linezolid; BTZ-043 and its metabolite M1; quabodepistat; and ganfeborole. No pharmacokinetic measurements will be performed in the HRZE control arm. Measured in ng/mL
At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
Minimum Observed Plasma Concentration of Study Drugs and Their Metabolites
Lasso di tempo: At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
The minimum observed plasma concentration (Cmin) will be estimated using non-compartmental analysis for the applicable study drugs and metabolites in each treatment arm. These include TBAJ-587 and its metabolites M2, M3 and M12; pretomanid; linezolid; BTZ-043 and its metabolite M1; quabodepistat; and ganfeborole. No pharmacokinetic measurements will be performed in the HRZE control arm. Measured as ng/mL.
At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
Time to Maximum Observed Plasma Concentration of Study Drugs and Their Metabolites
Lasso di tempo: At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
The time to maximum observed plasma concentration (Tmax) will be estimated using non-compartmental analysis for the applicable study drugs and metabolites in each treatment arm. These include TBAJ-587 and its metabolites M2, M3 and M12; pretomanid; linezolid; BTZ-043 and its metabolite M1; quabodepistat; and ganfeborole. No pharmacokinetic measurements will be performed in the HRZE control arm. Measured in hours.
At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
Area Under the Plasma Concentration-Time Curve From 0 to 24 Hours for Study Drugs and Their Metabolites
Lasso di tempo: At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B
The area under the plasma concentration-time curve from 0 to 24 hours (AUC0-24) will be estimated using non-compartmental analysis for the applicable study drugs and metabolites in each treatment arm. These include TBAJ-587 and its metabolites M2, M3 and M12; pretomanid; linezolid; BTZ-043 and its metabolite M1; quabodepistat; and ganfeborole. No pharmacokinetic measurements will be performed in the HRZE control arm. Measured as ng-h/mL
At Day 15 and Week 8 for participants in Part A and at Day 15 for participants in Part B

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Sputum Mycobacterial Load Measured Using the Molecular Bacterial Load Assay From Baseline Through Week 8
Lasso di tempo: From baseline to the end of treatment at 8 weeks
The Molecular Bacterial Load Assay (MBLA) measures viable Mycobacterium tuberculosis in sputum by quantifying mycobacterial ribosomal RNA. Mycobacterial load will be expressed as estimated colony-forming units per millilitre (eCFU/mL). The model-estimated change in log10-transformed mycobacterial load from baseline through Week 8 will be reported for each treatment arm. A decrease indicates a reduction in viable mycobacterial load. Measured as change in log10(eCFU/mL).
From baseline to the end of treatment at 8 weeks
Change in Sputum Lipoarabinomannan Concentration Measured Using the PATHFAST TB LAM Ag Assay From Baseline Through Week 8
Lasso di tempo: From baseline to the end of treatment at 8 weeks
The PATHFAST TB LAM Ag assay will be used to quantify lipoarabinomannan (LAM), a component of the Mycobacterium tuberculosis cell wall, in sputum. LAM concentration will be measured in picograms per millilitre. The model-estimated change in log10-transformed sputum LAM concentration from baseline through Week 8 will be reported for each treatment arm. A decrease indicates a reduction in sputum LAM concentration. Measured as change in log10(pg/mL).
From baseline to the end of treatment at 8 weeks
Change From Baseline in the TB27 Host Blood Transcriptomic Signature Score at Day 15
Lasso di tempo: From baseline before the first dose of study treatment to Day 15
The TB27 host transcriptomic signature will be measured in whole-blood samples collected at baseline and Day 15. The change in the TB27 signature score from baseline to Day 15 will be calculated for each participant. The TB27 signature is an RNA-based host-response marker intended to predict time to sputum culture conversion. Associations between changes in the TB27 signature score and microbiological markers will be analysed separately.
From baseline before the first dose of study treatment to Day 15
Minimum Inhibitory Concentration of Investigational Medicinal Products Against Mycobacterium tuberculosis Through Week 8
Lasso di tempo: From baseline before the first dose of study treatment to the end of treatment at Week 8, including the make-up or early-withdrawal visit where applicable
The minimum inhibitory concentration (MIC), defined as the lowest concentration of a study drug that inhibits growth of Mycobacterium tuberculosis, will be determined for applicable investigational medicinal products using isolates collected at baseline and during treatment. MIC values will be compared across assessment time points. A fourfold or greater increase from the baseline MIC will be considered a significant MIC shift and will trigger further testing as specified in the protocol. Measured as µg/mL.
From baseline before the first dose of study treatment to the end of treatment at Week 8, including the make-up or early-withdrawal visit where applicable
Mycobacterium tuberculosis Isolates With Resistance-Associated Mutations Following a Fourfold or Greater MIC Increase
Lasso di tempo: From baseline before the first dose of study treatment to the end of treatment at Week 8, including the make-up or early-withdrawal visit where applicable
Whole-genome sequencing will be performed on post-baseline Mycobacterium tuberculosis isolates showing a fourfold or greater increase from baseline in the minimum inhibitory concentration of a study drug. Sequencing will assess mutations associated with resistance to study drugs. Results will be reported as the number of sequenced isolates in which one or more resistance-associated mutations are identified.
From baseline before the first dose of study treatment to the end of treatment at Week 8, including the make-up or early-withdrawal visit where applicable
Association Between Individual Drug Exposure and Change in Log10-Transformed Sputum Culture Time to Positivity Through Week 8
Lasso di tempo: From baseline to the end of treatment at Week 8; pharmacokinetic exposure is assessed at Day 15 and Week 8 in Part A and at Day 15 in Part B
Individual drug exposure will be estimated using pharmacokinetic samples collected at Day 15 and Week 8 in Part A and at Day 15 in Part B. Exposure-response modelling will assess the relationship between estimated drug exposure and the change in log10-transformed sputum culture time to positivity from baseline through Week 8. Increasing time to positivity indicates a reduction in viable mycobacterial load.
From baseline to the end of treatment at Week 8; pharmacokinetic exposure is assessed at Day 15 and Week 8 in Part A and at Day 15 in Part B

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Fairoez Ryklief, MBBChB, TASK Clinical Trials

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

23 luglio 2026

Completamento primario (Stimato)

30 dicembre 2027

Completamento dello studio (Stimato)

30 dicembre 2027

Date di iscrizione allo studio

Primo inviato

21 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 agosto 2026

Primo Inserito (Effettivo)

19 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

19 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

Plan not yet available

Periodo di condivisione IPD

Immediately after publication.

Criteri di accesso alla condivisione IPD

Not available yet

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .