En studie för att lära dig mer om studiemedicinen Aztreonam-Avibactam (ATM-AVI) hos spädbarn och nyfödda inlagda på sjukhus med bakteriell infektion (CHERISH) (CHERISH)
En fas 2a, 2-delad, öppen, icke-randomiserad, multicenter, engångs- och multipeldosstudie för att utvärdera farmakokinetik, säkerhet och tolerabilitet av Aztreonam och Avibactam ± Metronidazol hos nyfödda och spädbarn från födseln till yngre än 9 månaders ålder med Misstänkta eller bekräftade infektioner på grund av gramnegativa patogener som kräver intravenös antibiotikabehandling
The purpose of this study is to learn about the safety and effects of ATM-AVI for the possible treatment of infections caused by a type of bacteria called gram-negative bacteria.
The study medicine is a combination of an antibiotic, aztreonam (ATM), and another medicine, avibactam (AVI), which is used to help stop bacteria from being resistant to antibiotics. Antibiotics are medicines that fights bacteria and infections.
The study will include newborns and infants up to 9 months of age who are admitted in the hospital.
The study is conducted in 2 parts: Part A and Part B.
In Part A, all participants will receive a single intravenous (injected directly into a vein) infusion of ATM-AVI. This is to study the safety and effects of a single amount.
In Part B, all participants will receive multiple intravenous infusions of ATM-AVI as treatment for a possible or confirmed infection with gram-negative bacteria.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This is a 2-part Phase 2a, non-randomized, multicenter, open-label, single and multi-dose study to assess pharmacokinetics (PK), safety, and tolerability of ATM-AVI in hospitalized neonates and infants aged birth, including preterm birth, to <9 months. A total of 48 participants will be enrolled in 4 age cohorts of 12 each, 6 Part A and 6 Part B. Part A will begin enrolling before Part B and no infant may participate in both parts. Cohort 1 will include full term infants age ≥13 weeks to <39 weeks and preterm infants postmenstrual age ≥50 weeks to <75 weeks. Cohort 2 will include full term infants age ≥28 weeks to <13 weeks and preterm infants postmenstrual age ≥40 weeks to <50 weeks and ≥28 days of age. Cohort 3 will include full term infants age birth to <28 days. Cohort 4 will include preterm infants age birth to <28 days or postmenstrual age <40 weeks.
Participants in Part A must be hospitalized and receiving intravenous antibiotic treatment for a suspected or confirmed bacterial infection. Participants will receive a single 3 hour intravenous infusion of ATM-AVI and have 3 ATM-AVI blood level assessments during and up to 5 hour after the infusion. Participants will be observed for 48 hours following the infusion to assess safety and toleration and will have a final follow-up safety assessment which may be conducted by telephone 4-5 weeks following the infusion. The single infusion of ATM-AVI is administered to assess the safety, tolerability, and pharmacokinetics of a single dose of ATM-AVI and is not intended as treatment for the bacterial infection. The total duration of study participation in Part A is expected to be 5 weeks through the end of the final safety follow-up.
Participants in Part B must be hospitalized with suspected or confirmed aerobic gram-negative bacterial infection requiring intravenous antibacterial therapy. Part B participants will receive multiple 3 hour intravenous infusions of ATM-AVI every 6 hour (8 hours for preterm infants) for 3-14 days as treatment for their bacterial infection and to assess ATM-AVI pharmacokinetics, safety, tolerability, and efficacy. Participants with complicated intra-abdominal infection (cIAI) will also receive intravenous metronidazole and all participants will have the option to receive other intravenous antibiotic treatment for gram-positive bacteria, as appropriate. Participants who have a good clinical response after 72 hours of intravenous ATM-AVI treatment may be switched to a different orally administered antibiotic, if clinically appropriate. Part B participants will have a total of 5 ATM-AVI blood level assessments over the first 2 or more days following the start of ATM-AVI infusions and will have their clinical response assessed at the End of Treatment (intravenous and oral, if applicable), and at a Test-of-Cure (TOC) evaluation 7 to 14 days after the last antibiotic treatment (intravenous or oral). A final safety assessment which may be conducted by telephone will occur 4-5 weeks after the last dose of ATM-AVI. The total duration of study participation in Part B is expected to be up to 7 weeks through the end of the final safety follow-up.
Additional safety monitoring will be provided by an independent external Data Monitoring Committee (DMC). Enrollment for the study will begin with Part A, single dose, cohorts 1-3. Part A Cohort 4 (preterm neonates) will commence enrollment after sponsor and DMC review of plasma drug levels and safety for a least 2 participants in Part A Cohort 3 and review of ATM-AVI safety and tolerability for all participants enrolled at that time. Enrollment in the multidose Part B cohorts will be delayed until preliminary information is obtained regarding ATM-AVI multidose safety, tolerability, and drug levels for the participants 9 months to 2 years of age in the separate ongoing ATM-AVI pediatric study C3601008 [NCT05639647].
Studietyp
Inskrivning (Beräknad)
Fas
- Fas 2
Kontakter och platser
Studiekontakt
- Namn: Pfizer CT.gov Call Center
- Telefonnummer: 1-800-718-1021
- E-post: ClinicalTrials.gov_Inquiries@pfizer.com
Studieorter
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Buenos Aires
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Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina, 1039
- Rekrytering
- Sanatorio Sagrado Corazón
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Mar del Plata, Buenos Aires, Argentina, 7600
- Rekrytering
- Clinica Del Niño Y La Madre
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Córdoba Province
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Córdoba, Córdoba Province, Argentina, X5000IIH
- Rekrytering
- Clinica Privada del Sol S.A
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Tucumán Province
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San Miguel de Tucumán, Tucumán Province, Argentina, 4000
- Rekrytering
- Hospital del Niño Jesús
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Burgas, Bulgarien, 8000
- Rekrytering
- UMHAT Deva Maria
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Rousse, Bulgarien, 7002
- Rekrytering
- Umhat Kanev
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California
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Orange, California, Förenta staterna, 92868
- Rekrytering
- Children's Hospital of Orange County
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Orange, California, Förenta staterna, 92868
- Rekrytering
- Children's Hospital of Orange County Southwest Tower
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Colorado
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Aurora, Colorado, Förenta staterna, 80045
- Rekrytering
- Children's Hospital Colorado
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Indiana
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Indianapolis, Indiana, Förenta staterna, 46202
- Rekrytering
- Riley Hospital for Children at Indiana University Health
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Kentucky
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Louisville, Kentucky, Förenta staterna, 40202
- Rekrytering
- Norton Children's Hospital
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Louisville, Kentucky, Förenta staterna, 40202
- Rekrytering
- Novak Center for Children's Health
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Louisville, Kentucky, Förenta staterna, 40202
- Rekrytering
- University of Louisville, Norton Children's Research Institute
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Massachusetts
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Boston, Massachusetts, Förenta staterna, 02111
- Rekrytering
- Tufts Medical Center
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North Carolina
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Durham, North Carolina, Förenta staterna, 27710
- Rekrytering
- Duke University - Main Hospital and Clinics
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Texas
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Houston, Texas, Förenta staterna, 77030
- Rekrytering
- The University of Texas Health Science Center at Houston
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Houston, Texas, Förenta staterna, 77030
- Rekrytering
- Memorial Hermann Hospital - Texas Medical Center
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Kentrikí Makedonía
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Thessaloniki, Kentrikí Makedonía, Grekland, 546 42
- Har inte rekryterat ännu
- Ippokrateio General Hospital of Thessaloniki
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Gujarat
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Surat, Gujarat, Indien, 395002
- Rekrytering
- Nirmal Hospital Pvt Ltd.
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Karnataka
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Bengaluru, Karnataka, Indien, 560074
- Rekrytering
- RajaRajeswari Medical College and Hospital
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Maharashtra
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Pune, Maharashtra, Indien, 411006
- Rekrytering
- Sahyadri Super Speciality Hospital
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Uttar Pradesh
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Lucknow, Uttar Pradesh, Indien, 226030
- Rekrytering
- Medanta Hospital Lucknow
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West Bengal
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Kolkata, West Bengal, Indien, 700017
- Rekrytering
- Institute of Child Health
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Central District
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Petah Tikva, Central District, Israel, 49202
- Rekrytering
- Schneider Children's Medical Center
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Northern District
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Haifa, Northern District, Israel, 3109601
- Rekrytering
- Rambam Health Care Campus
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Florence
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Florence, Florence, Italien, 50139
- Rekrytering
- Azienda Ospedaliera Universitaria Meyer IRCCS
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Madrid, Spanien, 28041
- Har inte rekryterat ännu
- Hospital Universitario 12 de Octubre
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Madrid, Comunidad de
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Madrid, Madrid, Comunidad de, Spanien, 28046
- Rekrytering
- Hospital Universitario La Paz
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Taichung, Taiwan, 407
- Rekrytering
- Taichung Veterans General Hospital
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Taoyuan, Taiwan, 33305
- Rekrytering
- Chang Gung Medical Foundation Linkou Chang Gung Memorial Hospital
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Hsinchu
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Hsinchu, Hsinchu, Taiwan, 300046
- Rekrytering
- Hsinchu Municipal Mackay Children's Hospital
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Hualien
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Hualien City, Hualien, Taiwan, 970
- Rekrytering
- Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria
Participants must meet the following key inclusion criteria to be eligible for enrollment into the study:
- Hospitalized with age from birth <9 months, including preterm birth
- Part A: Receiving IV antibiotics for treatment of suspected or confirmed bacterial infection, including but not limited to cIAI, cUTI, HAP/VAP, BSI, or sepsis.
- Part B: Suspected or confirmed gram-negative bacterial infection requiring IV antibiotics, including but not limited to cIAI, cUTI, HAP/VAP, BSI, or sepsis.
Participants with any of the following characteristics/conditions will be excluded:
- Received any other investigational medicinal product within the longer of 30 days or 5 half-lives before enrollment.
- Any medical or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
- Severe renal impairment or known significant renal disease, as evidenced by elevated serum creatinine at screening, or urinary output <0.5 mL/kg/h for 6 consecutive hours or requirement for dialysis.
- Part B Only: Received >24 hours of systemic antibiotic treatment for gram-negative organisms at time of enrollment, unless documented treatment failure or lack of improvement in at least one objective sign or symptom of infection after ≥48 hours of antibiotics.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Grundläggande vetenskap
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Part A, Cohorts 1-4
Single dose pharmacokinetics. |
Single intravenous infusion of aztreonam-avibactam over 3 hours to assess pharmacokinetics, safety, and toleration. |
|
Experimentell: Part B, Cohorts 1-4
Multi-dose pharmacokinetics and treatment |
Multiple intravenous infusions of aztreonam-avibactam over 3 hours, repeated every 6-8 hours up to 14 days to assess pharmacokinetics, safety, toleration, and efficacy. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Maximum Predicted Plasma Concentration (Cmax) of ATM and AVI
Tidsram: Up to Day 15
|
Cmax is the maximum plasma concentration of ATM and AVI as population pharmacokinetic (popPK) analysis predicts. |
Up to Day 15
|
|
Area under the Concentration-Time Curve (AUC) of ATM-AVI
Tidsram: Up to Day 15
|
AUC is a measure of the plasma concentration of ATM and AVI overtime as popPK analysis predicts. |
Up to Day 15
|
|
Plasma Elimination Half-Life (t1/2)
Tidsram: Up to Day 15
|
Half-life is the time measured for the plasma concentration of ATM and AVI to decrease by one half as popPK analysis predicts. |
Up to Day 15
|
|
Apparent Clearance (CL)
Tidsram: Up to Day 15
|
ATM and AVI clearance is a quantitative measure of the rate at which ATM and AVI are removed from the blood (rate at which ATM and AVI are metabolized or eliminated by normal biological processes). Clearance obtained after intravenous infusion dose (apparent clearance) is influenced by the fraction of the dose absorbed. |
Up to Day 15
|
|
Plasma concentrations of ATM and AVI by nominal sampling time
Tidsram: Up to Day 15
|
Plasma concentrations of ATM and AVI on Day 1 and at steady state (Day 2 or later) will be summarized by the nominal sampling time using descriptive statistics (eg number, mean, standard deviation). |
Up to Day 15
|
|
Proportion of Participants reporting Adverse Events (AE)
Tidsram: Baseline up to Day 50
|
Proportion of participant AE reports of vital signs, physical examinations, and clinical laboratory tests overall and by age cohort. For each AE the last assessment made prior to the first dose of study drug will be defined as the baseline. |
Baseline up to Day 50
|
|
Proportion of Participants reporting Serious Adverse Events (SAE)
Tidsram: Baseline up to Day 50
|
Proportion of participant SAE reports of vital signs, physical examinations, and clinical laboratory tests overall and by age cohort. For each SAE the last assessment made prior to the first dose of study drug will be defined as the baseline. |
Baseline up to Day 50
|
|
Proportion of Participants reporting AEs leading to discontinuation of study drug
Tidsram: Baseline up to Day 50
|
Proportion of Participants reporting AEs leading to discontinuation of study drug from baseline. For each discontinuation the last assessment made prior to the first dose of study drug will be defined as the baseline. |
Baseline up to Day 50
|
|
Proportion of Participants reporting AEs resulting in death
Tidsram: Baseline up to Day 50
|
Proportion of Participants reporting AE resulting in death from baseline. For each death the last assessment made prior to the first dose of study drug will be defined as the baseline. |
Baseline up to Day 50
|
|
Proportion of Participants reporting liver injury and acute kidney injury
Tidsram: Baseline up to Day 50
|
Proportion of Participants reporting liver injury and acute kidney injury from baseline. For each report of liver and acute kidney injury the last assessment made prior to the first dose of study drug will be defined as the baseline. |
Baseline up to Day 50
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Part B: Proportion of participants with each clinical outcome and with a favorable clinical outcome at end of IV study treatment (EOIV)
Tidsram: Up to 15 days after start of IV study treatment
|
Clinical Cure is defined baseline signs and symptoms improved such that no further antimicrobial treatment is required for an aerobic gram-negative baseline infection. Participants who receive treatment for gram-positive organisms or adjunctive therapy for Pseudomonas aeruginosa, as allowed per protocol, can still have a response of cure. Clinical improvement is defined as baseline signs and symptoms sufficiently improved to allow switching to an oral antibiotic treatment. A favorable outcome is clinical cure or clinical improvement. Failure is defined as a requirement for further antibiotic treatment, including following premature discontinuation due to an adverse event, or death after receiving at least 48 hours of treatment. Indeterminant is defined as data not available for evaluation of efficacy for any reason. |
Up to 15 days after start of IV study treatment
|
|
Part B: Proportion of participants with each clinical outcome and with a favorable clinical outcome at end of treatment (EOT)
Tidsram: Within 48 hours after last dose of oral switch treatment
|
EOT is only applicable for participants switched to an oral antibiotic treatment. Possible outcomes are cure, failure, or indeterminant. |
Within 48 hours after last dose of oral switch treatment
|
|
Part B: Proportion of participants with each clinical outcome and with a favorable clinical outcome at test of cure (TOC)
Tidsram: 7-14 days after the last study treatment
|
Possible outcomes are cure, failure, or indeterminant. |
7-14 days after the last study treatment
|
|
Part B: Proportion of participants with a favorable microbiological response at TOC
Tidsram: 7-14 days after the last study treatment
|
A favorable response is eradication or presumed eradication. Eradication is absence of the causative pathogen from an appropriately obtained specimen at the site of infection. Presumed eradication is when a repeat culture was not performed and the clinical response is cure. |
7-14 days after the last study treatment
|
|
Part B: Counts and proportions of pathogens with each per-pathogen microbiological response at EOIV/EOT
Tidsram: Up to 15 days after start of IV study treatment
|
Possible outcomes are eradication, presumed eradication, persistence, presumed persistence or indeterminate. Presumed eradication/persistence based on repeat culture not performed and clinical outcome of cure/failure. Persistence is the causative pathogen is still present from an appropriately obtained specimen at the site of the infection. Indeterminant includes participant lost to follow-up or death after receiving less than 48 hours of study treatment. |
Up to 15 days after start of IV study treatment
|
|
Part B: Counts and proportions of pathogens with each per-pathogen microbiological response at TOC
Tidsram: 7-14 days after the last study treatment
|
Possible outcomes are eradication, presumed eradication, persistence, presumed persistence or indeterminate. |
7-14 days after the last study treatment
|
|
Part B: Counts and proportions of participants with emergent infections (new infections or superinfections) during the study
Tidsram: Through study completion, up to Day 50
|
Superinfection is defined as emergence of a new pathogen associated with worsening signs and symptoms of infection and a requirement for additional antibiotics during the period up to and including EOIV/EOT. New infection is defined as emergence of a new pathogen associated with worsening signs and symptoms of infection and a requirement for additional antibiotics during the period after EOIV/EOT. |
Through study completion, up to Day 50
|
Samarbetspartners och utredare
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- C3601010
- 2023-507757-15-01 (Registeridentifierare: CTIS (EU))
- 2023 (U.S.S. NIH-anslag/kontrakt)
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
IPD-planbeskrivning
Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests.
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