TREAT-GNB [CR-GNB]

Status: Recruiting
Location: See all (41) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

TREAT-GNB is an innovative trial to expedite the evaluation of various antibiotic choices and treatment strategies for severe multidrug-resistant Gram-negative bacterial infections, specifically bloodstream and lower respiratory tract infections. This approach combines platform trial elements with adaptive clinical designs to streamline the evaluation of various treatment options and optimise resource utilisation. The overall aim of the TREAT-GNB platform trial is to identify interventions that improve survival in patients with severe infections due to Gram-negative bacteria. In the CR-GNB silo of TREAT-GNB, the primary objective is to quantify the effect on all-cause mortality at 28 days of a range of interventions in patients with bloodstream infections, ventilator-associated pneumonia, and hospital-acquired pneumonia caused by CR-GNB.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ A: Bloodstream infections

⁃ a) Suitable for at least 2 antibiotic regimens in the site randomisation list

• Growth of Gram-negative bacilli identified from blood culture(s)

• Receiving or planning to receive intravenous antibiotics

• Expected time from blood culture sampling to randomisation is ≤ 96 hours.

⁃ OR

⁃ B: Ventilator-associated pneumonia / hospital-acquired pneumonia a) Suitable for at least 2 antibiotic regimens in the site randomisation list b) Infection syndrome definitions\^( (US Centers for Disease Control and Prevention National Healthcare Safety Network)3: i) At least one of the following:

• temperature \> 38 °C

• white blood cell count ≥ 12,000 cells/mm3 (12 x 109/L, 12 x 103/µL) or ≤ 4,000 cells/mm3 (4 x 109/L, 4 x 103/µL)

• altered mental status with no other causes in \> 70 years old; AND ii) Two or more chest imaging tests demonstrating at least one of the following:

⁃ 1\) new and progressive OR progressive and persistent infiltrate 2) new and persistent OR progressive and persistent consolidation 3) new and persistent OR progressive and persistent cavitation; AND iii) At least two of the following:

• new onset of purulent sputum, or change in character of sputum, or increased respiratory secretions, or increased in suctioning requirements

• new onset or worsening tachypnoea or dyspnoea

• rales or bronchial breath sounds

• worsening gas exchange defined by oxygen desaturations (e.g., PaO2/FiO2 \< 240), increased oxygen requirements or increased ventilation demand.

• c) Hospital admission \> 48 hours d) Predominant growth of Gram-negative bacilli identified from respiratory tract specimen(s)\*; e) Receiving or planning to receive intravenous antibiotics f) Expected time from respiratory culture sampling to randomisation is ≤ 96 hours

• AND

• C: CR-GNB antibiotic backbone domain

• a) Gram-negative bacilli belonging to Acinetobacter baumannii-calcoaceticus complex, Pseudomonas aeruginosa or Enterobacterales b) Carbapenem resistance in isolate detected - i) Phenotypically via conventional microbiology testing: meropenem / imipenem / ertapenem resistance; OR ii) Genotypically via PCR or next generation sequencing: presence of genes associated with carbapenemase production (eg. blaNDM, blaKPC, blaIMP, blaIMI, blaVIM, blaOXA-48-like).

Locations
Other Locations
Australia
Princess Alexandra Hospital
NOT_YET_RECRUITING
Brisbane
Royal Brisbane and Women's Hospital
NOT_YET_RECRUITING
Brisbane
China
The First Affiliated Hospital, Zhejiang University School of Medicine
NOT_YET_RECRUITING
Hangzhou
The Second Affiliated Hospital, Xi'an Jiang Tong University
NOT_YET_RECRUITING
Xi'an
Xuzhou First People's Hospital
NOT_YET_RECRUITING
Xuzhou
Lebanon
American University of Beirut Medical Center
NOT_YET_RECRUITING
Beirut
Malaysia
Ampang Hospital
NOT_YET_RECRUITING
Ampang
Queen Elizabeth I
NOT_YET_RECRUITING
Kota Kinabalu
Queen Elizabeth II
NOT_YET_RECRUITING
Kota Kinabalu
Miri Sarawak Hospital
NOT_YET_RECRUITING
Miri
Hospital Sungai Buloh
NOT_YET_RECRUITING
Sungai Buloh
Qatar
Hamad Medical Corporation
NOT_YET_RECRUITING
Doha
Saudi Arabia
King Saud bin Abdulaziz University for Health Sciences
NOT_YET_RECRUITING
Riyadh
Singapore
National University Hospital
RECRUITING
Singapore
South Africa
Helen Joseph Hospital
NOT_YET_RECRUITING
Johannesburg
Spain
Hospital General Universitario Dr. Balmis
NOT_YET_RECRUITING
Alicante
Hospital Universitario de Badajoz
NOT_YET_RECRUITING
Badajoz
Hospital Universitario de Cruces
NOT_YET_RECRUITING
Barakaldo
Hospital del Mar Barcelona
NOT_YET_RECRUITING
Barcelona
Hospital Universitario Bellvitge
NOT_YET_RECRUITING
Barcelona
Hospital Universitario Reina Sofía Córdoba
NOT_YET_RECRUITING
Córdoba
Hospital Universitario San Cecilio
NOT_YET_RECRUITING
Granada
Hospital Universitario Virgen de las Nieves
NOT_YET_RECRUITING
Granada
Hospital Clínico San Carlos
NOT_YET_RECRUITING
Madrid
Hospital General Universitario Gregorio Marañón
NOT_YET_RECRUITING
Madrid
Hospital Universitario de La Princesa
NOT_YET_RECRUITING
Madrid
Hospital Universitario La Paz
NOT_YET_RECRUITING
Madrid
Hospital Regional Universitario de Málaga
NOT_YET_RECRUITING
Málaga
Hospital Universitario Virgen de la Victoria
NOT_YET_RECRUITING
Málaga
Hospital Álvaro Cunqueiro
NOT_YET_RECRUITING
Pontevedra
Hospital Universitario de Donostia
NOT_YET_RECRUITING
San Sebastián
Hospital Universitario Marqués de Valdecilla
NOT_YET_RECRUITING
Santander
Hospital Universitario Virgen de Valme
NOT_YET_RECRUITING
Seville
Hospital Universitario Virgen del Rocío
NOT_YET_RECRUITING
Seville
Hospital Universitario Virgen Macarena
NOT_YET_RECRUITING
Seville
Hospital Clínico Universitario Lozano Blesa
NOT_YET_RECRUITING
Zaragoza
Thailand
Phramongkutkloa Hospital
NOT_YET_RECRUITING
Bangkok
Rajavithi Hospital
NOT_YET_RECRUITING
Bangkok
Maharaj Nakorn Chiang Mai Hospital, Chiangmai University
NOT_YET_RECRUITING
Chiang Mai
Turkey
İstanbul Medipol Üniversitesi
NOT_YET_RECRUITING
Istanbul
United Arab Emirates
Dubai Hospital
NOT_YET_RECRUITING
Dubai
Contact Information
Primary
Yin Mo, MBBS, PhD
mdcmy@nus.edu.sg
+65 65164988
Time Frame
Start Date: 2025-04-21
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 600
Treatments
Active_comparator: Colistin/Polymyxin B + Sulbactam
Active_comparator: Colistin/Polymyxin B + Tigecycline/Eravacycline
Active_comparator: Colistin/Polymyxin B + Meropenem
Active_comparator: Ceftazidime-avibactam + Sulbactam
Active_comparator: Ceftazidime-avibactam + Fosfomycin
Active_comparator: Ceftazidime-avibactam
Active_comparator: Ceftazidime-avibactam + Aztreonam
Active_comparator: Ceftazidime-avibactam + Colistin/Polymyxin B
Active_comparator: High-dose meropenem
Active_comparator: Meropenem + Fosfomycin
Active_comparator: Meropenem-vaborbactam
Active_comparator: Cefiderocol
Active_comparator: Ceftolozane-tazobactam
Active_comparator: Ceftolozane-tazobactam + Meropenem
Related Therapeutic Areas
Sponsors
Leads: National University of Singapore
Collaborators: European Clinical Research Alliance for Infectious Diseases (ECRAID), The University of Queensland

This content was sourced from clinicaltrials.gov

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