- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07587684
A Study of IN026 in Participants With Refractory Gout
A Clinical Study on the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of IN026 in the Treatment of Refractory Gout
The goal of this clinical study is to learn if IN026 Injection is safe and works to lower uric acid levels in adults with refractory gout (gout that does not respond well to standard treatments). The main questions it aims to answer are:
- What medical problems do participants have when taking IN026, such as changes in vital signs, blood tests, or heart rhythm?
- How does the body absorb, process, and respond to IN026, and does it trigger an immune reaction?
- Does IN026 lower uric acid levels in the blood and reduce tophi?
Investigator will start with lower doses of IN026 and slowly increase the dose to find the well-tolerated dose.
Participants will:
- Receive IN026 through an intravenous (IV) drip into a vein at a set dose.
- Complete a screening period of up to 4 weeks, followed by treatment and check-ups for up to 20 weeks.
- Have blood and urine samples taken at set times to check safety and how the body responds to IN026.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
- Navn: QiuBai Li Union Hospital, Tongji Medical College, Huazhong University of
- Telefonnummer: +86-27-85726338
- E-mail: qiubaili@hust.edu.cn
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Can voluntarily sign the informed consent form (ICF) and comply with ICF and study protocol requirements.
- Male or female, 18-75 years old (inclusive) at screening.
- Meet 2015 ACR/EULAR gout classification criteria, in the intercritical phase of gout or acute flare resolved ≥2 weeks at screening.
- Serum uric acid ≥420 μmol/L (7 mg/dl) at screening.
- Meet the definition of refractory gout (poor uric acid control accompanied by severe gout symptoms)
Exclusion Criteria:
- Gout secondary to radiotherapy/chemotherapy, lead poisoning, organ transplantation, tumor, etc. at screening/baseline.
- Rheumatoid arthritis, infectious/septic arthritis, or other acute inflammatory arthritis at screening/baseline.
- Glucose-6-phosphate dehydrogenase (G6PD) deficiency history, or G6PD level below normal lower limit.
- Positive HBsAg; HCV antibody positive is excluded except those with sustained HCV-RNA negativity after standard treatment; HIV antibody positive; active syphilis.
- Presence of chronic liver diseases including active hepatitis, cirrhosis and alcoholic liver disease.
- Participants with a history of any of the following: serious cardiovascular diseases within 6 months prior to screening; or serious diseases of the digestive, respiratory, urinary, musculoskeletal, neuropsychiatric, hematological, or immune systems within 3 months prior to screening.
- Prolonged QTcF at screening.
- Uncontrolled or untreated hypertension at screening.
- Participants who have received medications that may affect endpoint assessment, such as other urate-lowering therapies, mRNA-LNP vaccine, PEGylated drugs and uricase agents.
- History of severe allergy, or known allergy to IN026 or its components.
- Participation in other clinical trials within 30 days prior to screening.
- Participants with poor compliance, or those deemed otherwise unsuitable for this study by the investigator.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Sekventiel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: IN026 at Dose-Level A
Participants receive intravenous IN026 Injection at dose-level A on Week 1 Day 1 (W1D1).
Following safety/tolerability assessment, participants may receive extra doses (up to 5 in total) at predefined frequency.
|
IN026 Injection is a lipid nanoparticle (LNP)-formulated mRNA therapeutic administered as an intravenous (IV) infusion
|
|
Eksperimentel: IN026 at Dose-Level B
Participants receive intravenous IN026 Injection at dose-level B on Week 1 Day 1 (W1D1).
Following safety/tolerability assessment, participants may receive extra doses (up to 5 in total) at predefined frequency.
|
IN026 Injection is a lipid nanoparticle (LNP)-formulated mRNA therapeutic administered as an intravenous (IV) infusion
|
|
Eksperimentel: IN026 at Dose-Level C
Participants receive intravenous IN026 Injection at dose-level C on Week 1 Day 1 (W1D1).
Following safety/tolerability assessment, participants may receive extra doses (up to 5 in total) at predefined frequency.
|
IN026 Injection is a lipid nanoparticle (LNP)-formulated mRNA therapeutic administered as an intravenous (IV) infusion
|
|
Eksperimentel: IN026 at Dose-Level D
Participants receive intravenous IN026 Injection at dose-level D on Week 1 Day 1 (W1D1).
Following safety/tolerability assessment, participants may receive extra doses (up to 5 in total) at predefined frequency.
|
IN026 Injection is a lipid nanoparticle (LNP)-formulated mRNA therapeutic administered as an intravenous (IV) infusion
|
|
Eksperimentel: IN026 at Dose-Level E
Participants receive intravenous IN026 Injection at dose-level E on Week 1 Day 1 (W1D1).
Following safety/tolerability assessment, participants may receive extra doses (up to 5 in total) at predefined frequency.
|
IN026 Injection is a lipid nanoparticle (LNP)-formulated mRNA therapeutic administered as an intravenous (IV) infusion
|
|
Eksperimentel: IN026 at Dose-Level F
Participants receive intravenous IN026 Injection at dose-level F on Week 1 Day 1 (W1D1).
Following safety/tolerability assessment, participants may receive extra doses (up to 5 in total) at predefined frequency.
|
IN026 Injection is a lipid nanoparticle (LNP)-formulated mRNA therapeutic administered as an intravenous (IV) infusion
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Incidence of Adverse Events (AEs), Treatment-Emergent Adverse Events (TEAEs), and Serious Adverse Events (SAEs)
Tidsramme: From first dose (Week 1 Day 1) through end of study (Week 21)
|
From first dose (Week 1 Day 1) through end of study (Week 21)
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change from Baseline in Serum Uric Acid Concentration
Tidsramme: From baseline (Week 1 Day 1) through Week 21
|
From baseline (Week 1 Day 1) through Week 21
|
|
Change in Tophi from Baseline
Tidsramme: From baseline (Week 1 Day 1) through Week 21
|
From baseline (Week 1 Day 1) through Week 21
|
|
Plasma Concentration of IN026 mRNA Over Time
Tidsramme: At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
|
Plasma Concentration of Ionizable Lipid SX-66 Over Time
Tidsramme: At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
|
Serum Uricase Level Over Time
Tidsramme: At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
|
Serum Uric Acid Level Over Time
Tidsramme: At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
|
Serum Allantoin Level Over Time
Tidsramme: At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
|
Titer of Anti-Drug Antibodies (ADAs) Over Time
Tidsramme: At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
At pre-specified timepoints from first dose (Week 1 Day 1) through Week 21
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: QiuBai Li, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Krystalarthropatier
- Muskuloskeletale sygdomme
- Patologiske processer
- Gigt
- Ledsygdomme
- Purin-Pyrimidin metabolisme, medfødte fejl
- Metabolisme, medfødte fejl
- Genetiske sygdomme, medfødte
- Bindevævssygdomme
- Medfødte, arvelige og neonatale sygdomme og abnormiteter
- Patologiske tilstande, tegn og symptomer
- Ernæringsmæssige og metaboliske sygdomme
- Hud- og bindevævssygdomme
- Gigt
- Hyperurikæmi
- Metaboliske sygdomme
- Reumatiske sygdomme
Andre undersøgelses-id-numre
- IN026-001
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
produkt fremstillet i og eksporteret fra U.S.A.
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Ildfast gigt
-
Nantes University HospitalTrukket tilbageCD22+ Relapsed/Refractory B-ALLFrankrig
-
Samsung Medical CenterAfsluttetHER2-positiv Refractory Advanced CancerKorea, Republikken
-
European Society for Blood and Marrow TransplantationMallinckrodtAfsluttetSteroid Refractory GVHDSpanien, Det Forenede Kongerige, Sverige, Italien, Israel, Frankrig, Danmark, Tyskland, Polen, Kalkun, Rumænien, Belgien, Grækenland, Den Russiske Føderation
-
Shanghai Pudong HospitalUTC Therapeutics Inc.Trukket tilbageMesothelin-positive Advanced Refractory Solid TumorsKina
-
Cellenkos, Inc.Ikke rekrutterer endnuSteroid Refractory Graft Versus Host Disease
-
ElsaLys BiotechIkke rekrutterer endnu
-
MaaT PharmaRekrutteringSteroid Refractory GVHD | Tarm GVHDFrankrig
-
Yi-Lun WangAfsluttetSteroid Refractory GVHDTaiwan
-
Changhai HospitalRui Therapeutics Co., LtdRekrutteringRelapseret/Refraktær Immun Nefropati | Relapsed/Refractory Immune-mediated Kidney DiseaseKina
-
Fujian Cancer HospitalIkke rekrutterer endnuHawthorn Red Kombineret Refractory Cancer Smerter
Kliniske forsøg med IN026 Injection
-
Jiangsu HengRui Medicine Co., Ltd.Ikke rekrutterer endnu
-
Grand Medical Pty Ltd.Aktiv, ikke rekrutterende
-
Beijing Boren HospitalAfsluttetAvanceret solid tumor | Recidiverende/refraktær lymfomKina
-
Ruijin HospitalShanghai Essight Bio Co.,LtdRekruttering
-
Staidson (Beijing) Biopharmaceuticals Co., LtdAfsluttetAcute respiratory distress syndromKina
-
Shengjing HospitalJiangsu HengRui Medicine Co., Ltd.RekrutteringHR Positiv/HER2 lav brystkræftKina
-
Jeffrey S HeierKato Pharmaceuticals, Inc.AfsluttetVitreomakulær trækkraft | Vitreomakulær vedhæftning | Vitreomakulær vedhæftningForenede Stater
-
Jiangsu Kanion Pharmaceutical Co., LtdBeijing Bionovo Medicine Development Co., Ltd.Afsluttet
-
Bio-Thera SolutionsAfsluttet
-
GE HealthcareRekrutteringOnkologi | Ondartet fast tumorHolland