Phase
Condition
Kidney Disease
Focal Segmental Glomerulosclerosis
Treatment
GSK4771261
Placebo matching GSK4771261
Clinical Study ID
Ages 25-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
For Part A
Body weight greater than or equal to (>=) 45 kilograms (kg) and basal metabolicindex (BMI) within the range 19.5 to 32 kilograms per square meters (kg/m^2),inclusive
Capable of giving signed informed consent,
Participants who are overtly healthy as determined by medical evaluation by theinvestigator or a medically qualified designee based on medical history, physicalexamination, laboratory tests, and cardiac monitoring
Women must be of non-childbearing potential
For Part B (planned Cohorts 1-3 and optional cohorts 4-5):
Body weight >=45 kg and BMI within the range 19.5 to 32 kg/m^2, inclusive.
Capable of giving signed informed consent, Confirmed diagnosis of Autosomal dominantpolycystic kidney disease (ADPKD) by either applicable guidelines and/or genetic andimaging screening assessments
Participants diagnosed with ADPKD may have complications or comorbidities directlyrelated to ADPKD but should be otherwise healthy as determined by the investigatoror medically qualified designee based on a medical evaluation including medicalhistory, physical examination, laboratory tests clinical testing
Confirmation of known ADPKD causal genetic mutation(s) at the Polycystic kidneydisease (PKD)1 and/or PKD2 loci based on genetic testing at screening and/orexisting genetic information collected during the participant's routine clinicalcare for ADPKD from a genetic testing provider that, in the judgement of theinvestigator, is clinically valid.
Mayo imaging classification groups 1C, 1D or 1E as assessed using the informationcollected at screening
Estimated glomerular filtration rate (eGFR) greater than or equal to (>=) 45milliliters per minutes per 1.73 square meters (mL/min/1.73m^2) (based on theChronic kidney disease- Epidemiology Collaboration [CKD-EPI 2021] eGFR equation) andis not anticipated by the participant's regular treating physician to have asustained decline by greater than (>)10 percent (%) over the following 12 months
Intolerant of tolvaptan treatment, unwilling to initiate tolvaptan treatment orineligible for tolvaptan treatment for ADPKD
A female participant is eligible to participate if she is not pregnant orbreastfeeding and agrees to use birth control methods as discussed with the studydoctor.
Woman of childbearing potential (WOCBP) and Woman of non-childbearing potential (WONCBP) must have a negative highly sensitive pregnancy test prior to the Magneticresonance imaging (MRI) scan being performed in the screening period of Part B
A WOCBP and WONCBP must have a negative highly sensitive pregnancy test (urine orserum as required by local regulations) within 24 hours before the first dose ofstudy intervention For Part B (additional inclusion criteria for optional cohorts 4-5 only)
eGFR >=30 mL/min/1.73m^2 (based on the CKD-EPI 2021 eGFR equation) and, in theclinical judgement of the investigator, the participant:
has been clinically stable for the 24 months before screening; and,
is not anticipated by the participant's regular treating physician to have asustained decline in kidney function by >10% over the following 12 months; and,
is not anticipated to need renal replacement therapy in the next 12 months; and,
does not have any other clinical, biochemical or familial feature at screening thatsuggests a clinically significant decline in kidney function is anticipated in thenext 12 months.
Exclusion
Exclusion Criteria:
For Part A:
History or presence of cardiovascular, respiratory, hepatic, renal,gastrointestinal, endocrine, hematological, or neurological disorders capable ofsignificantly altering the absorption, metabolism, or elimination of drugs;constituting a risk when taking the study drug; or interfering with theinterpretation of data.
History of malignancy of any type.
History of kidney disease or kidney abnormalities or eGFR less than (<) 90milliliters per minute per 1.73 square meters (mL/min/1.73m^2) (based on the chronickidney disease- Epidemiology Collaboration [CKD-EPI] 2021 eGFR equation) atscreening.
Use of prescription or non-prescription drugs, including vitamins, herbal anddietary supplements (including St John's Wort) within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study drug and for the duration ofstudy participation.
QT interval corrected (QTc)>450 milliseconds (msec)
Participation in this study would result in loss of blood or blood products inexcess of 500 mL within 56 days
Current enrolment or past participation in an investigational clinical trial inwhich an investigational medicinal product was administered within the followingtime periods prior to the first dosing day of the current study: 30 days, 5half-lives or twice the duration of the biological effect of the investigationalproduct, whichever is longer
Exposure to more than 4 investigational medicinal products within 12 months prior todosing
Significant allergy to humanized monoclonal antibodies
Clinically significant multiple or severe drug allergies, or severe post-treatmenthypersensitivity reactions (including, but not limited to, erythema multiformemajor, linear Immunoglobulin A (IgA) dermatosis, toxic epidermal necrolysis, andexfoliative dermatitis)
Pregnant or lactating female
Current or previous diagnosis of diabetes mellites (DM) (Type 1 or Type 2)
Glycosylated hemoglobin (HbA1c) >=48 millimoles per mole (mmol/mol) (>=6.5%) atscreening
Bone fracture within 6 months prior to screening, or presence of a known unresolvedor incompletely resolved fracture
Positive pre-clinical study drug/alcohol screen, including tetrahydrocannabinol
Positive Human Immunodeficiency Virus (HIV) antibody test
Evidence of Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection,as determined by local diagnostic procedures
Evidence at screening of clinically significant hematological disorder (affectinghemoglobin, red blood cells [RBC], White blood cells [WBC] or platelets) or abnormalblood clotting parameters
Regular use of recreational drugs, including substances containingtetrahydrocannabinol
Participants who are unable to refrain from smoking, vaping or using other tobaccoproducts during study visits or overnight stays
Poor peripheral venous access by visual inspection (intravenous [IV] administrationcohort(s) only)
Average weekly intake of greater than (>) 14 United Kingdom (UK) units of alcohol.One UK unit is equivalent to 8 grams (g) of alcohol: a half-pint (approximately 240mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits
Sensitivity to any of the study interventions, or components thereof, or drug orother allergy that, in the opinion of the investigator [or medical monitor],contraindicates participation in the study
Use of any products intended to treat medical conditions that are not approved bythe governing health authority in a given country or region (for example, herbalmedicine, health supplements, traditional medicine, homeopathic remedies, etc.)
Alanine transaminase (ALT) >1.5x Upper Limit of Normal (ULN)
Total bilirubin >1.5xULN; Participants with Gilbert's syndrome can be included withtotal bilirubin <=3.0xULN as long as direct bilirubin is <=1.0xULN
Current or chronic history of liver disease or known hepatic or biliaryabnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones)
Presence of hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody (HBcAb) at screening or within 3 months prior to first dose of study intervention
Positive hepatitis C antibody test result at screening or within 3 months prior tofirst dose of study intervention
Positive hepatitis C Ribonucleic acid (RNA) test result at screening or within 3months prior to first dose of study intervention
Part B:
Presence of active, clinically significant cardiovascular, respiratory, hepatic,gastrointestinal, endocrine (including, but not limited to, incompletely controlledsecondary or tertiary hyperparathyroidism and clinically significant vitamin Ddeficiency), hematological (including, but not limited to, transfusion-dependentanemia), bone (including, but not limited to, osteoporosis), or neurologicaldisorders, with the exception of ADPKD, capable of significantly altering theabsorption, metabolism, or elimination of drugs; constituting a risk when taking thestudy drug; or interfering with the interpretation of data
Clinically significant abnormal blood pressure (BP), that is, if the participant isnot taking antihypertensive therapy: systolic BP >=160 millimeters of mercury (mmHg)and/or diastolic BP >=90mmHg; or If the participant is established on a stableregimen of antihypertensive drug(s): on-treatment systolic BP >=160 mmHg and/ordiastolic BP >=90mmHg
Lymphoma, leukemia, or any malignancy within the past 5 years except for basal cellor squamous epithelial carcinomas of the skin that have been resected with noevidence of recurrence or metastatic disease for 3 years
Breast cancer within the past 10 years
Use of prescription and non-prescription drugs, including vitamins A, B, C, E, K,herbal and dietary supplements (including St John's Wort) within 7 days or 5half-lives (whichever is longer) prior to the first dose of study drug and for theduration of study participation. Paracetamol, at doses of <=4 gram per 24 hour (g/24h) is permitted for use at any time during the study
Contraindication to, or unwillingness to undergo, MRI scanning (e.g., presence ofMRI-incompatible metal implant)
Congenital absence of one kidney
Kidney cyst interventions such as cyst aspiration or cyst fenestration within 12weeks prior to screening and during the screening period, or such interventionsplanned or anticipated within the follow-up period
Acute symptomatic kidney cyst hemorrhage or infection within 12 weeks prior toscreening
Evidence of current, chronic, or recurrent kidney or liver cyst infection
Estimated proteinuria >1g/24 hour at screening and/or pre-dose (day -7 to day -1)
Abnormal urinalysis suggestive of clinically significant glomerular disease orurinary tract infection
Presence of known clinically significant renal or hepatic calculi, or symptomsthereof, at screening
Treatment with tolvaptan within 6 months prior to screening
Presence of an incompletely healed wound at screening and/or planned surgicalprocedure that would occur during study.
Participation in this study would result in loss of blood or blood products inexcess of 500 mL within 56 days
Current enrolment or past participation in an investigational clinical trial inwhich an investigational medicinal product was administered within the followingtime periods prior to the first dosing day of the current study: 30 days, 5half-lives or twice the duration of the biological effect of the investigationalproduct, whichever is longer
Exposure to more than 4 investigational medicinal products within 12 months prior todosing
Significant allergy to humanized monoclonal antibodies
Clinically significant multiple or severe drug allergies, or severe post-treatmenthypersensitivity reactions (including, but not limited to, erythema multiformemajor, linear Immunoglobulin A (IgA) dermatosis, toxic epidermal necrolysis, andexfoliative dermatitis)
Pregnant or lactating female
Current or previous diagnosis of diabetes mellites (DM) (Type 1 or Type 2)
HbA1c >=48 millimoles per mole (mmol/mol) (>=6.5%) at screening
Bone fracture within 6 months prior to screening, or presence of a known unresolvedor incompletely resolved fracture
Positive pre-clinical study drug/alcohol screen, including tetrahydrocannabinol
Positive HIV antibody test
Evidence of SARS-CoV-2 infection, as determined by local diagnostic procedures
Evidence at screening of clinically significant hematological disorder (affectinghemoglobin, RBC, WBC or platelets) or abnormal blood clotting parameters
Regular use of recreational drugs, including substances containingtetrahydrocannabinol
Participants who are unable to refrain from smoking, vaping or using other tobaccoproducts during study visits or overnight stays
Poor peripheral venous access by visual inspection (IV administration cohort(s)only)
Average weekly intake of greater than (>) 14 UK units of alcohol. One UK unit isequivalent to 8 grams of alcohol: a half-pint (approximately240 mL) of beer, 1 glass (125 mL) of wine or 1 (25 mL) measure of spirits
Sensitivity to any of the study interventions, or components thereof, or drug orother allergy that, in the opinion of the investigator [or medical monitor],contraindicates participation in the study
Use of any products intended to treat medical conditions that are not approved bythe governing health authority in a given country or region (for example, herbalmedicine, health supplements, traditional medicine, homeopathic remedies, etc.)
Alanine transaminase (ALT) >1.5x Upper Limit of Normal (ULN)
Total bilirubin >1.5xULN; Participants with Gilbert's syndrome can be included withtotal bilirubin <=3.0xULN as long as direct bilirubin is <=1.0xULN
Current or chronic history of liver disease or known hepatic or biliaryabnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones)
Presence of HBsAg and/or HBcAb at screening or within 3 months prior to first doseof study intervention
Positive hepatitis C antibody test result at screening or within 3 months prior tofirst dose of study intervention
Positive hepatitis C RNA test result at screening or within 3 months prior to firstdose of study intervention
QTc >450 milliseconds (msec) or QTc >480 msec for participants with bundle branchblock
Study Design
Connect with a study center
GSK Investigational Site
Bruxelles, 1200
BelgiumActive - Recruiting
GSK Investigational Site
Gent, 9000
BelgiumSite Not Available
GSK Investigational Site
Leuven, 3000
BelgiumActive - Recruiting
GSK Investigational Site
London, Ontario N6A 5A5
CanadaActive - Recruiting
GSK Investigational Site
MontrEal, Quebec H4J 1C5
CanadaActive - Recruiting
GSK Investigational Site
Brest, 29200
FranceActive - Recruiting
GSK Investigational Site
Paris, 75015
FranceSite Not Available
GSK Investigational Site
Koeln, Nordrhein- Westfalen 50937
GermanySite Not Available
GSK Investigational Site
Luebeck, Schleswig-Holstein 23538
GermanySite Not Available
GSK Investigational Site
Berlin, 10117
GermanySite Not Available
GSK Investigational Site
Groningen, 9713 GZ
NetherlandsSite Not Available
GSK Investigational Site
Leiden, 2333 ZA
NetherlandsSite Not Available
GSK Investigational Site
Rotterdam, 3015 GD
NetherlandsSite Not Available
GSK Investigational Site
Barcelona, 08035
SpainActive - Recruiting
GSK Investigational Site
Madrid, 28041
SpainActive - Recruiting
GSK Investigational Site
Cambridge, CB2 0GG
United KingdomActive - Recruiting
GSK Investigational Site
Hammersmith, W12 0HS
United KingdomSite Not Available
GSK Investigational Site
London, NW3 2QG
United KingdomActive - Recruiting
GSK Investigational Site
Newcastle Upon Tyne, NE7 7DN
United KingdomSite Not Available
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