Lupus NephritisPhase 2NCT05097989
Study of ALXN2050 in Proliferative Lupus Nephritis (LN) or Immunoglobulin A Nephropathy (IgAN)
A Phase 2 study testing ALXN2050 in people with Lupus Nephritis and Immunoglobulin A Nephropathy, run by Alexion Pharmaceuticals, Inc. at 71 sites in 16 countries.
Trial summary
This is a Phase 2, randomized, double-blind, placebo-controlled, multicenter study of ALXN2050 (120 and 180 milligrams [mg]) in addition to background therapy consistent with the standard of care in adult participants (≥ 18 to ≤ 75 years of age) with either LN or IgAN. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Lupus Nephritis, Immunoglobulin A Nephropathy, IgAN
- What is being tested?
- ALXN2050
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 100 participants
- Where
- 71 sitesin 16 countries
- Study dates
- 14 Jan 2022to 9 Dec 2024
- Phase
- Phase 2
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Both Cohorts
- Participants on sodium-glucose cotransporter-2 (SGLT 2) inhibitors (eg, empagliflozin) must be on a stable dose for ≥ 3 months with no planned change in dose during the Blinded Treatment Periods (through Week 50).
- LN Cohort
- Clinical diagnosis of SLE by 2019 American College of Rheumatology and European League Against Rheumatism criteria.
- Diagnosis of 2018 Revised International Society of Nephrology/Renal Pathology Society classification (active focal or diffuse proliferative LN Class III or IV) confirmed by biopsy obtained ≤ 6 months prior to Screening or during Screening Period. Participants may co-exhibit Class V disease. Participants with de novo or relapsing disease may be eligible.
- Clinically active LN at Screening requiring/receiving immunosuppression induction treatment in the opinion of the Investigator.
Show all 13Show fewer
- Proteinuria with UPCR ≥ 1 g/g based on one 24 hour urine collection during the Screening Period.
- IgAN Cohort
- Established diagnosis of primary IgAN based on kidney biopsy obtained any time prior to or during the Screening Period.
- Mean proteinuria ≥ 1 g/day on 2 complete and valid 24 hour urine collections during the Screening Period.
- For participants with a kidney biopsy performed > 1 year prior to Screening that was used for eligibility: Presence of hematuria as defined by a positive result for blood on urine dipstick or ≥ 10 red blood cells (RBCs)/high power field (hpf) microscopy on urine sediment (documented by the local laboratory) during Screening Period. Presence of hematuria documented by the central laboratory may also be acceptable.
- Compliance with stable and optimal dose of RAS inhibitor treatment including maximum allowed or tolerated ACE inhibitor and/or ARB dose for ≥ 3 months prior to Screening with no expected change in dose during the Blinded Treatment Periods (through Week 50) (participants with established intolerance to RAS inhibitors may be included).
- Controlled and stable blood pressure (defined as < 140/90 millimeters of mercury [mmHg]) over the past 3 months prior to randomization.
Who cannot join
- Both Cohorts
- eGFR ≤ 30 milliliters/minute/1.73 squared meters during Screening calculated by Chronic Kidney Disease Epidemiology Collaboration.
- For participants with eGFR < 45 mL/min/1.73 m2 at Screening, presence of any of the following in glomeruli on most recent kidney biopsy prior to or during the Screening
- Period:
- ≥ 50% interstitial fibrosis and tubular atrophy
- ≥ 50% glomerular sclerosis
Show all 27Show fewer
- ≥ 50% active crescent formation
- Concomitant significant renal disease other than LN or IgAN on the most recent biopsy prior to or during the Screening Period.
- History of solid organ or bone marrow transplant, or planned transplant during the Blinded Extended Treatment Period (50 weeks).
- Splenectomy or functional asplenia.
- Known or suspected complement deficiency, unless attributable to underlying disease (that is, LN and IgAN).
- Bone marrow insufficiency with absolute neutrophil count < 1.3 × 10^3/microliter; thrombocytopenia (platelet count < 50,000/cubic millimeter).
- LN Cohort
- Participants who have initiated any of the following treatments for the current active LN flare:
- Cyclophosphamide ≤ 6 months prior to Screening
- CNIs ≤ 1 months prior to Screening
- A cumulative dose of intravenous (IV) methylprednisolone > 3 g
- Mycophenolate mofetil > 2 g/day (or equivalent) for ≥ 8 consecutive weeks prior to Screening
- Prednisone or prednisone equivalent ≥ 0.5 mg/kg/day for ≥ 8 consecutive weeks prior to Screening
- Uncontrolled hypertension (systolic blood pressure > 160 mmHg or diastolic blood pressure > 110 mmHg) on 2 or more measurements during the Screening Period.
- Prior history or clinically active SLE-related cerebritis, seizures, stroke, or stroke syndrome requiring treatment or clinically active pericarditis
- Inability to take or tolerate the standard of care background therapies
- IgAN Cohort
- Diagnosis of rapid progressive glomerulonephritis as measured by eGFR loss ≥ 30% over a period of 3 months prior to or during the Screening Period.
- Secondary etiologies of IgAN.
- Prednisone or prednisone equivalent > 20 mg/day for > 14 consecutive days or any other systemic immunosuppression for the treatment of IgAN ≤ 6 months prior to Screening
- Blood pressure of ≥ 140/90 mmHg during the Screening Period confirmed on 2 measures > 30 minutes apart.
Trial locations and contacts
71 sites in 16 countries.
71 sites in 16 countries
United States10 sites
Research Site
Albuquerque, New Mexico, 87106
Research Site
Des Moines, Iowa, 50309
Research Site
Gainesville, Florida, 32603
Research Site
Houston, Texas, 77054
Research Site
Huntsville, Alabama, 35805
Research Site
Kansas City, Missouri, 64111
Research Site
Loma Linda, California, 92350
Research Site
Nampa, Idaho, 83687
Research Site
New York, New York, 10016
Research Site
Northridge, California, 91324
Spain8 sites
Research Site
Barcelona, 08025
Research Site
Barcelona, 8003
Research Site
Córdoba, 14004
Research Site
Girona, 17007
Research Site
L'Hospitalet de Llobregat, 08907
Research Site
Palma de Mallorca, 07120
Research Site
Seville, 41013
Research Site
Valencia, 46026
United Kingdom7 sites
Research Site
Bristol, BS105NB
Research Site
Cambridge, CB2 0QQ
Research Site
Doncaster, DN2 5LT
Research Site
Leicester, LE5 4PW
Research Site
London, E1 1BB
Research Site
London, SE5 9RS
Research Site
Manchester, M13 9WL
Brazil6 sites
Research Site
Belo Horizonte, 30150-221
Research Site
Curitiba, 80030-110
Research Site
Juiz de Fora, 36010-570
Research Site
Porto Alegre, 90035-003
Research Site
Porto Alegre, 90480-000
Research Site
Salvador, 40150-150
Germany6 sites
Research Site
Berlin, 10117
Research Site
Essen, 45122
Research Site
Mainz A. Rhein, 55131
Research Site
Mannheim, 68135
Research Site
Marburg, 30625
Research Site
München, 81377, DE
Italy5 sites
Research Site
Bari, 70124
Research Site
Brescia, 25123
Research Site
Milan, 20132
Research Site
Naples, 80131
Research Site
Torino, 10154
Argentina4 sites
Research Site
Ciudad de Buenos Aires, C1015ABO
Research Site
Córdoba, 5000
Research Site
La Plata, B1902COS
Research Site
Rosario, S2000DEJ
Australia4 sites
Research Site
Clayton, 3168
Research Site
Liverpool, 2170
Research Site
Nedlands, 6009
Research Site
Westmead, 2145
Israel4 sites
Research Site
Ashkelon, 78306
Research Site
Haifa, 3109601
Research Site
Petah Tikva, 4941492
Research Site
Ramat Gan, 52621
Taiwan4 sites
Research Site
Kaohsiung City, 833
Research Site
New Taipei City, 220
Research Site
New Taipei City, 23561
Research Site
Taichung, 40705
China3 sites
Research Site
Guangzhou, 510080
Research Site
McKinney, 75069
Research Site
Shanghai, 200040
Mexico3 sites
Research Site
Guadalajara, 44140
Research Site
México, 11570
Research Site
Torreón, 27000
South Korea3 sites
Research Site
Busan, 49241
Research Site
Goyang-si, 10380
Research Site
Seoul, 03080
About this study
Official title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Dose-finding Study to Evaluate the Efficacy and Safety of ALXN2050 in Adult Participants With Proliferative Lupus Nephritis (LN) or Immunoglobulin A Nephropathy (IgAN)
This is a Phase 2, randomized, double-blind, placebo-controlled, multicenter study of ALXN2050 (120 and 180 milligrams [mg]) in addition to background therapy consistent with the standard of care in adult participants (≥ 18 to ≤ 75 years of age) with either LN or IgAN. The study will consist of an up to 6-week Screening Period, a 26-week blinded Initial Evaluation Period, a 24-week blinded Extended Treatment Period, and an Open-label Extension (OLE) Period of up to 2 years.
Safety will be monitored throughout the study.
- Conditions
- Lupus Nephritis, Immunoglobulin A Nephropathy, IgAN, LN
- Being tested
- ALXN2050, Placebo
- Keywords
- ALXN2050, Complement Factor D, Complement Alternative Pathway, LN, IgAN
- Medical subject headings
- Lupus Nephritis, Glomerulonephritis, IGA
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ALXN2050Drug
Also called ACH-0145228 (formerly)
Oral tablets
PlaceboDrug
Oral tablets
| Study group | Role | What they receive |
|---|---|---|
| LN Cohort: ALXN2050 180 mg | Experimental | Participants diagnosed with LN with an active flare will receive ALXN2050 in addition to standard-of-care background therapy. Receives: Drug: ALXN2050 |
| LN Cohort: ALXN2050 120 mg | Experimental | Participants diagnosed with LN with an active flare will receive ALXN2050 in addition to standard-of-care background therapy. Receives: Drug: ALXN2050 |
| LN Cohort: Placebo | Placebo comparator | Participants diagnosed with LN with an active flare will receive matched placebo in addition to standard-of-care background therapy. Receives: Drug: Placebo |
| IgAN Cohort: ALXN2050 180 mg | Experimental | Participants diagnosed with IgAN will receive ALXN2050 in addition to standard-of-care background therapy. Receives: Drug: ALXN2050 |
| IgAN Cohort: ALXN2050 120 mg | Experimental | Participants diagnosed with IgAN will receive ALXN2050 in addition to standard-of-care background therapy. Receives: Drug: ALXN2050 |
| IgAN Cohort: Placebo | Placebo comparator | Participants diagnosed with IgAN will receive matched placebo in addition to standard-of-care background therapy. Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Both Cohorts: Percentage Change in Proteinuria From Baseline at Week 26
Proteinuria, the presence of excess proteins in the urine, was assessed using 24-hour urine collections obtained at designated timepoints. A negative change from baseline indicated an improvement in symptoms.
Measured: Baseline, Week 26
Secondary outcomes (13)
Both Cohorts: Percentage Change in Proteinuria From Baseline at Week 50
Proteinuria, the presence of excess proteins in the urine, was assessed using 24-hour urine collections obtained at designated timepoints. A negative change from baseline indicated an improvement in symptoms.
Measured: Baseline, Week 50
Both Cohorts: Percentage of Participants Achieving >30% and >50% Reduction in Proteinuria at Week 26 and Week 50 Compared to Baseline
Proteinuria, the presence of excess proteins in the urine, was assessed using 24-hour urine collections obtained at designated timepoints. A reduction from baseline indicated an improvement in symptoms.
Measured: Week 26 and Week 50
Both Cohorts: Change From Baseline in Estimated Glomerular Filtration Rate (eGFR) at Week 26 and Week 50
Changes in kidney function were monitored using measurements of eGFR and calculated based on the Chronic Kidney Disease Epidemiology Collaboration formula. Results are reported in milliliters/minute/1.73 meters squared (mL/min/1.73 m^2). Estimates of change from baseline are least-square means based on a mixed-effect model for repeated measures model that included change from baseline as the response variable, treatment as independent variable and adjusts for covariates of baseline and the stratification factor at randomization. An increase in eGFR in response to treatment indicated an improvement in symptoms.
Measured: Baseline, Week 26 and Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Complete Renal Response at Week 26 and Week 50
Complete renal response was defined as a decrease in urine protein to creatinine ratio (UPCR) to ≤0.5 gram/gram (g/g), an eGFR rate >60 mL/min/1.73 m^2 or no eGFR reduction ≥20% from baseline, and no treatment failure. Treatment failure was defined as the receipt of additional standard of care therapy at any time during the study for protocol-defined renal flare, severe extrarenal systemic lupus erythematosus (SLE) flare, or suboptimal response.
Measured: Week 26 and Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Partial Renal Response at Week 26 and Week 50
Partial renal response was defined as a decrease in UPCR ≥50% compared to baseline, an eGFR rate >60 mL/min/1.73 m^2 or no eGFR reduction ≥20% from baseline, and no treatment failure. Treatment failure was defined as the receipt of additional standard of care therapy at any time during the study for protocol-defined renal flare, severe extrarenal SLE flare, or suboptimal response.
Measured: Week 26 and Week 50
LN Cohort: Time to the First Occurrence of UPCR ≤0.5 g/g as Measured by a Spot Urine Sample
UPCR was assessed using 24-hour urine collections obtained at designated time points. The time to the first occurrence of UPCR ≤0.5 g/g was summarized by spot urine sample analysis.
Measured: Up to Week 50
LN Cohort: Percentage of Participants Achieving Corticosteroid Taper to 7.5 mg/Day at Weeks 12, 26, and 50
A corticosteroid taper was carried out per protocol at the clinical discretion of the investigator.
Measured: Week 12, Week 26, And Week 50
LN Cohort: Percentage of Participants Experiencing a Renal Flare Through Week 50
Renal flare was determined in the opinion of the investigator and additional protocol-specified criteria. For participants who achieved a complete renal response, a renal flare was the reproducible recurrence of proteinuria ≥1g/g. For all other participants, a renal flare was either of the following: a reproducible increase of serum creatinine >25% higher than baseline or above the upper limit of normal (plus additional protocol-specified criteria) or a reproducible doubling of the UPCR from a 24-hour urine collection compared with the lowest previous value obtained after the first dose of study intervention.
Measured: Baseline Through Week 50
LN Cohort: Percentage of Participants Experiencing an Extrarenal SLE Flare Through Week 50
Extrarenal SLE flare was defined as an increase in the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) Safety of Estrogens in Lupus Erythematosus National Assessment modification ≥4 points that was not accounted for by proteinuria, hematuria, urinary cellular casts, hypocomplementemia, or an increase in anti-double-stranded DNA antibody level. The SLEDAI-2K is an instrument that was used to assesses the disease activity of extrarenal SLE flare across 18 disease descriptors. Each descriptor carried a weighted value ranging from 1-8, with the reported score calculated as the sum of these descriptors and ranging from 0 to 85. Higher scores represent increased degrees of disease activity.
Measured: Baseline Through Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Treatment Failure Through Week 50
Treatment failure was defined as the receipt of additional standard of care therapy at any time during the study for protocol-defined renal flare, severe extrarenal SLE flare, or suboptimal response.
Measured: Baseline through Week 50
LN Cohort: Change From Baseline in Serum Albumin at Week 26 and Week 50
For the determination of serum albumin, blood samples were obtained at designated time points. Results reported as grams/liter (g/L).
Measured: Baseline, Week 26 and Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Suboptimal Response Through Week 50
A suboptimal response was to be determined in the opinion of the investigator in addition to the following criterion: reproducible proteinuria ≤25% decreased compared to baseline based on UPCR on a 24-hour urine collection performed by a central laboratory.
Measured: Baseline Through Week 50
IgAN Cohort: Percentage of Participants Meeting the Criteria for Partial Remission at Week 26 And Week 50
Partial remission was defined as mean proteinuria <1 g/24 hours, based on two valid 24-hour urine collections obtained within 2 weeks prior to the study visit.
Measured: Week 26 and Week 50
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Oct 2021
- Study start14 Jan 2022
- Primary completion9 Dec 2024
- Study completion9 Dec 2024
Why it stopped: Sponsor Decision.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Lupus NephritisStudies of the same condition, open and under way.
- More trials run by Alexion Pharmaceuticals, Inc.The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- Alexion Pharmaceuticals, Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05097989
- Sponsor's protocol ID
- ALXN2050-NEPH-201
- Other IDs
- 2021-001426-22
- Status last verified
- Sep 2025
- First submitted
- 18 Oct 2021
- Last updated
- 15 Oct 2025
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Tunnicliffe DJ, Reid S, Craig JC, Samuels JA, Molony DA, Strippoli GF. Non-immunosuppressive treatment for IgA nephropathy. Cochrane Database Syst Rev. 2024 Feb 1;2(2):CD003962. doi: 10.1002/14651858.CD003962.pub3.
PubMed 38299639Avasare R, Drexler Y, Caster DJ, Mitrofanova A, Jefferson JA. Management of Lupus Nephritis: New Treatments and Updated Guidelines. Kidney360. 2023 Oct 1;4(10):1503-1511. doi: 10.34067/KID.0000000000000230.
PubMed 37528520
Study at a glance
From the registry record, last updated by the sponsor on 15 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 2, Randomized, Double-blind, Placebo-controlled, Dose-finding Study to Evaluate the Efficacy and Safety of ALXN2050 in Adult Participants With Proliferative Lupus Nephritis (LN) or Immunoglobulin A Nephropathy (IgAN)
- ClinicalTrials.gov ID
- NCT05097989
- Acronym / sponsor ID
- ALXN2050-NEPH-201
- Conditions
- Lupus Nephritis, Immunoglobulin A Nephropathy, IgAN, LN
- Keywords
- ALXN2050, Complement Factor D, Complement Alternative Pathway, LN, IgAN
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Sponsor Decision.
- Enrolment
- 100 participants (actual)
- Lead sponsor
- Alexion Pharmaceuticals, Inc.Industry (pharma, biotech, devices)
- Study start
- 14 Jan 2022 (actual)
- Primary completion
- 9 Dec 2024 (actual)
- Study completion
- 9 Dec 2024 (actual)
- First posted
- 28 Oct 2021 (actual)
- Results
- Posted 15 Oct 2025
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a Phase 2, randomized, double-blind, placebo-controlled, multicenter study of ALXN2050 (120 and 180 milligrams [mg]) in addition to background therapy consistent with the standard of care in adult participants (≥ 18 to ≤ 75 years of age) with either LN or IgAN. The study will consist of an up to 6-week Screening Period, a 26-week blinded Initial Evaluation Period, a 24-week blinded Extended Treatment Period, and an Open-label Extension (OLE) Period of up to 2 years.
Safety will be monitored throughout the study.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 6
| Arm | Type | Receives |
|---|---|---|
| LN Cohort: ALXN2050 180 mg | Experimental | Drug: ALXN2050Participants diagnosed with LN with an active flare will receive ALXN2050 in addition to standard-of-care background therapy. |
| LN Cohort: ALXN2050 120 mg | Experimental | Drug: ALXN2050Participants diagnosed with LN with an active flare will receive ALXN2050 in addition to standard-of-care background therapy. |
| LN Cohort: Placebo | Placebo comparator | Drug: PlaceboParticipants diagnosed with LN with an active flare will receive matched placebo in addition to standard-of-care background therapy. |
| IgAN Cohort: ALXN2050 180 mg | Experimental | Drug: ALXN2050Participants diagnosed with IgAN will receive ALXN2050 in addition to standard-of-care background therapy. |
| IgAN Cohort: ALXN2050 120 mg | Experimental | Drug: ALXN2050Participants diagnosed with IgAN will receive ALXN2050 in addition to standard-of-care background therapy. |
| IgAN Cohort: Placebo | Placebo comparator | Drug: PlaceboParticipants diagnosed with IgAN will receive matched placebo in addition to standard-of-care background therapy. |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (13 listed)
- Both Cohorts
- Participants on sodium-glucose cotransporter-2 (SGLT 2) inhibitors (eg, empagliflozin) must be on a stable dose for ≥ 3 months with no planned change in dose during the Blinded Treatment Periods (through Week 50).
- LN Cohort
- Clinical diagnosis of SLE by 2019 American College of Rheumatology and European League Against Rheumatism criteria.
- Diagnosis of 2018 Revised International Society of Nephrology/Renal Pathology Society classification (active focal or diffuse proliferative LN Class III or IV) confirmed by biopsy obtained ≤ 6 months prior to Screening or during Screening Period. Participants may co-exhibit Class V disease. Participants with de novo or relapsing disease may be eligible.
Key exclusion criteria (27 listed)
- Both Cohorts
- eGFR ≤ 30 milliliters/minute/1.73 squared meters during Screening calculated by Chronic Kidney Disease Epidemiology Collaboration.
- For participants with eGFR < 45 mL/min/1.73 m2 at Screening, presence of any of the following in glomeruli on most recent kidney biopsy prior to or during the Screening
- ≥ 50% interstitial fibrosis and tubular atrophy
- ≥ 50% glomerular sclerosis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ALXN2050Also: ACH-0145228 (formerly)Oral tablets | Drug | IgAN Cohort: ALXN2050 120 mg, IgAN Cohort: ALXN2050 180 mg, LN Cohort: ALXN2050 120 mg, LN Cohort: ALXN2050 180 mg |
| PlaceboOral tablets | Drug | IgAN Cohort: Placebo, LN Cohort: Placebo |
Primary outcome
Both Cohorts: Percentage Change in Proteinuria From Baseline at Week 26
Time frame: Baseline, Week 26
Proteinuria, the presence of excess proteins in the urine, was assessed using 24-hour urine collections obtained at designated timepoints. A negative change from baseline indicated an improvement in symptoms.
13 secondary outcomes
Both Cohorts: Percentage Change in Proteinuria From Baseline at Week 50
Time frame: Baseline, Week 50
Both Cohorts: Percentage of Participants Achieving >30% and >50% Reduction in Proteinuria at Week 26 and Week 50 Compared to Baseline
Time frame: Week 26 and Week 50
Both Cohorts: Change From Baseline in Estimated Glomerular Filtration Rate (eGFR) at Week 26 and Week 50
Time frame: Baseline, Week 26 and Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Complete Renal Response at Week 26 and Week 50
Time frame: Week 26 and Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Partial Renal Response at Week 26 and Week 50
Time frame: Week 26 and Week 50
LN Cohort: Time to the First Occurrence of UPCR ≤0.5 g/g as Measured by a Spot Urine Sample
Time frame: Up to Week 50
LN Cohort: Percentage of Participants Achieving Corticosteroid Taper to 7.5 mg/Day at Weeks 12, 26, and 50
Time frame: Week 12, Week 26, And Week 50
LN Cohort: Percentage of Participants Experiencing a Renal Flare Through Week 50
Time frame: Baseline Through Week 50
LN Cohort: Percentage of Participants Experiencing an Extrarenal SLE Flare Through Week 50
Time frame: Baseline Through Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Treatment Failure Through Week 50
Time frame: Baseline through Week 50
LN Cohort: Change From Baseline in Serum Albumin at Week 26 and Week 50
Time frame: Baseline, Week 26 and Week 50
LN Cohort: Percentage of Participants Meeting the Criteria for Suboptimal Response Through Week 50
Time frame: Baseline Through Week 50
IgAN Cohort: Percentage of Participants Meeting the Criteria for Partial Remission at Week 26 And Week 50
Time frame: Week 26 and Week 50
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 Oct 2025.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 38299639Tunnicliffe DJ, Reid S, Craig JC, Samuels JA, Molony DA, Strippoli GF. Non-immunosuppressive treatment for IgA nephropathy. Cochrane Database Syst Rev. 2024 Feb 1;2(2):CD003962. doi: 10.1002/14651858.CD003962.pub3.
- Derived from this study: PubMed 37528520Avasare R, Drexler Y, Caster DJ, Mitrofanova A, Jefferson JA. Management of Lupus Nephritis: New Treatments and Updated Guidelines. Kidney360. 2023 Oct 1;4(10):1503-1511. doi: 10.34067/KID.0000000000000230.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
71 sites in 16 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing ALXN2050 in people with Lupus Nephritis and Immunoglobulin A Nephropathy, run by Alexion Pharmaceuticals, Inc. at 71 sites in 16 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 13 inclusion and 27 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 15 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 71 sites in United States, Spain, United Kingdom, Brazil, Germany and 11 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 15 Oct 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Both Cohorts: Percentage Change in Proteinuria From Baseline at Week 26 (time frame: Baseline, Week 26). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05097989, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Oct 2025.