Ancient herbs meet modern viruses in fight against superbug pneumonia
NCT ID NCT07612605
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase trial will test a combination of a Chinese herbal formula (Yiqi Huoxue Jiedu) and bacteriophages (viruses that target bacteria) in 250 people with severe pneumonia caused by drug-resistant bacteria. The goal is to see if this combo can clear the infection faster and reduce deaths. The study is not yet recruiting.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Yiqi Huoxue Jiedu formula (herbal mix) and bacteriophages (viruses that kill bacteria)
- What this could lead to
- If it works, this could point toward a new way to treat severe pneumonia caused by drug-resistant bacteria, potentially lowering death rates.
- What could go wrong
- This is a very early (Phase 1) trial, so safety and effectiveness are not yet proven. The combination therapy may not work better than standard care, and side effects are unknown.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 250 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients who meet the diagnostic criteria for severe pneumonia caused by drug-resistant Gram-negative bacilli and conform to the TCM syndrome differentiation of Qi deficiency, toxin accumulation and blood stasis syndrome; * Patients confirmed by rapid on-site microbiological evaluation (M-ROSE), clinical microbial culture and drug susceptibility testing (based on the drug susceptibility test results of our hospital or other Grade A tertiary hospitals) to be infected with multidrug-resistant Klebsiella pneumoniae, Acinetobacter baumannii or Pseudomonas aeruginosa; * Aged 18 to 85 years old; * Patients or their family members agree to cooperate with the collection of upper and lower respiratory tract specimens, consent to bronchoscopy plus bronchoalveolar lavage, and agree to receive nebulized inhalation of bacteriophage therapy; * Patients or their family members have fully read, understood and signed the informed consent form. Exclusion Criteria: * Women who are pregnant or lactating; * Patients with immunodeficiency; * Patients receiving immunosuppressive therapy or suffering from immunodeficiency diseases; * Patients who have received mechanical ventilation for more than 60 days prior to enrollment; * Patients with active pulmonary tuberculosis, lung abscess, or Grade D chronic obstructive pulmonary disease (COPD); * Patients with incomplete sampling or clinical data; * Patients with known allergies to bacteriophage products or the components of Yiqi Huoxue Jiedu Formula; * Patients judged by the researchers as unsuitable for participation in this study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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1st Medical Center of Chinese PLA General Hospital
Beijing, China
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8th Medical Center of Chinese PLA General Hospital
Beijing, China
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The First Affiliated Hospital of Guangzhou Medical University
Guangdong, Guangzhou, China
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The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Guangdong, Guangzhou, China
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Other studies related to the condition(s) this trial covers.
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