A nurse in blue scrubs checks the blood pressure of a smiling woman in a pink shirt at a clinic.

IgA Nephropathy Treatments Compared

6 FDA-approved drugs and 5 in development, side by side from the current prescribing labels. Newest label Aug 2026. Checked October 1, 2026.

Full approval, kidney functionTarpeyo · Filspari · Fabhalta
Accelerated approval, proteinuriaVanrafia · Trutakna · Voyxact

Six drugs are FDA-approved specifically for IgA nephropathy, all since December 2021, and they divide into 2 tiers. Tarpeyo, Filspari and Fabhalta hold full approval to slow the loss of kidney function, with eGFR results on their labels. Vanrafia, Trutakna and Voyxact hold accelerated approval based on lowering protein in the urine, and their labels say it is not yet established that they slow kidney decline, although Trutakna and Voyxact have since reported positive 2-year eGFR results. Four are pills, Trutakna is a weekly self-injection and Voyxact is a self-injection every 4 weeks. Five more drugs are in Phase 3 or under FDA review, with decisions on povetacicept and Ultomiris expected before the end of 2026.

Side by side

6 approved IgA nephropathy treatments at a glance

How each drug is given, how often, who it is approved for and when it was first approved, from the current FDA label.

IgA Nephropathy treatments compared: route, schedule, approved use and approval date
DrugHow it is givenHow oftenApproved forFirst approved
budesonide delayed-release capsules
Calliditas Therapeutics
Capsule by mouth once a day, for a 9-month course16 mg once daily in the morning for 9 months, then 8 mg once daily for the last 2 weeksAdults with primary IgAN at risk of disease progression, to reduce loss of kidney functionDecember 15, 2021
sparsentan
Travere Therapeutics
Tablet by mouth once a day200 mg once daily for 14 days, then 400 mg once daily; must stop ACE inhibitors and ARBs firstAdults with primary IgAN at risk of disease progression, to slow kidney function declineFebruary 17, 2023
iptacopan
Novartis
Capsule by mouth twice a day200 mg twice daily, with or without food; vaccination against encapsulated bacteria at least 2 weeks before startingAdults with primary IgAN at risk of disease progression, to slow kidney function declineAugust 7, 2024
atrasentan
Novartis
Tablet by mouth once a day0.75 mg once daily, with or without food; pregnancy must be ruled out before startingAdults with primary IgAN at risk of rapid progression (generally UPCR 1.5 g/g or higher), to reduce proteinuriaApril 2, 2025
atacicept-vymj
Vera Therapeutics
Shot under the skin once a week, self-injected at home150 mg subcutaneously once weekly with an autoinjector, in the abdomen or thighAdults with primary IgAN at risk of disease progression, to reduce proteinuriaJuly 7, 2026
sibeprenlimab-szsi
Otsuka
Shot under the skin once every 4 weeks, self-injected at home400 mg subcutaneously once every 4 weeks with a prefilled syringe, in the thigh or abdomenAdults with primary IgAN at risk of disease progression, to reduce proteinuriaNovember 25, 2025
The calendar

A year on each IgA nephropathy treatment

Every dose in a year, drawn to the label schedule, so the difference between a daily pill and a twice-yearly infusion is the picture.

Tarpeyo
By mouth, at home
16 mg once daily in the morning for 9 months, then 8 mg once daily for the last 2 weeks (no fixed yearly count)
Filspari
By mouth, at home
365 doses a year
Fabhalta
By mouth, at home
730 doses a year
Vanrafia
By mouth, at home
365 doses a year
Trutakna
Injection, at home
52 doses a year
Voyxact
Injection, at home
13 doses a year

Counts follow the label schedule for a full year on the maintenance dose. Drugs given in cycles or adjusted to blood tests have no fixed count, so their schedule is written out instead.

The evidence

What the pivotal IgA nephropathy trials showed

The primary result from the trial each FDA approval rests on, as reported on the label.

IgA Nephropathy pivotal trial results by drug
DrugPivotal trialPrimary result
budesonide delayed-release capsules
Calliditas Therapeutics
NefIgArd, 364 adults in the efficacy analysis (389 treated)
Trial record or paper
At 2 years, eGFR was 5.9 mL/min/1.73 m2 better than placebo; at 9 months UPCR was 31% lower than placebo
sparsentan
Travere Therapeutics
PROTECT, 404 adults
Trial record or paper
UPCR fell 45% vs 15% on irbesartan at week 36 (35% relative reduction); eGFR declined 1.2 mL/min/1.73 m2 per year less over 110 weeks
iptacopan
Novartis
APPLAUSE-IgAN, 477 adults
Trial record or paper
eGFR declined 3.0 vs 5.7 mL/min/1.73 m2 per year on placebo over 24 months (2.8 per year difference); UPCR 38% lower than placebo at 9 months
atrasentan
Novartis
ALIGN, 403 adults (270 in the primary analysis)
Trial record or paper
UPCR fell 38% vs 3% on placebo at week 36 (36% reduction vs placebo)
atacicept-vymj
Vera Therapeutics
ORIGIN 3, 428 adults (203 in the primary analysis)
Trial record or paper
UPCR fell 46% vs 7% on placebo at week 36 (42% reduction vs placebo)
sibeprenlimab-szsi
Otsuka
VISIONARY, 510 adults (320 in the interim analysis)
Trial record or paper
UPCR fell 50% vs a 2% rise on placebo at month 9 (51% reduction vs placebo)
Safety

IgA Nephropathy treatment side effects and warnings

Filspari, Fabhalta and Vanrafia carry a boxed warning, the FDA's strongest. The rest list their main precautions.

IgA Nephropathy treatments: most common side effects and key warnings from the FDA labels
DrugMost common side effectsKey warning
budesonide delayed-release capsules
Calliditas Therapeutics
peripheral edema 17%, hypertension 12% and muscle spasms 12%No boxed warning. Steroid effects: adrenal suppression (taper when stopping), higher infection risk, and worsening of high blood pressure or diabetes.
sparsentan
Travere Therapeutics
hyperkalemia 17%, hypotension 16% and peripheral edema 16%Boxed warning Boxed warning: liver toxicity and birth defects. Liver tests every 3 months and pregnancy must be ruled out; available only through the Filspari REMS program.
iptacopan
Novartis
abdominal pain 8%, dizziness 5% and nausea 4%Boxed warning Boxed warning: serious infections from encapsulated bacteria (meningococcal, pneumococcal, Hib). Vaccination required; available only through the Fabhalta REMS program.
atrasentan
Novartis
peripheral edema 10%, anemia 6% and liver transaminase elevation 2%Boxed warning Boxed warning: birth defects. Contraindicated in pregnancy; effective contraception required. Also liver toxicity and fluid retention.
atacicept-vymj
Vera Therapeutics
infections 32% (28% on placebo), injection site reactions 30% (5% on placebo) and upper respiratory tract infection 12%No boxed warning. Higher infection risk; no live vaccines within 30 days before or during treatment.
sibeprenlimab-szsi
Otsuka
infections 49% (45% on placebo), injection site reactions 24% (23% on placebo) and upper respiratory infection 15%No boxed warning. Higher infection risk; no live vaccines within 30 days before or during treatment.
Not yet approved

IgA nephropathy treatments in Phase 3 or under FDA review

Investigational drugs with a Phase 3 trial, shown separately because their results are not from a label. Status as of the date in each row.

IgA Nephropathy drugs in development
DrugStatusHow it works and is givenPivotal trialResult so farWhat is next
Vertex Pharmaceuticals (Alpine Immune Sciences)
Under FDA reviewas of October 1, 2026Dual BAFF and APRIL blocker (engineered TACI fusion protein) that lowers harmful IgA productionShot under the skin every 4 weeks (80 mg); planned as a home autoinjectorRAINIER, Phase 3, 605 peoplePrimary endpoint: UPCR change at week 36 (interim); eGFR slope through week 104 (final)
ClinicalTrials.gov
Met primary endpoint: UPCR fell 52.0% vs 4.3% on placebo at week 36, a 49.8% reduction vs placebo in 199 people (Vertex press release, 2026-03-09)FDA decision date (PDUFA) November 30, 2026, for accelerated approval
Vertex press release, June 1, 2026
Alexion (AstraZeneca)
Under FDA reviewas of October 1, 2026Long-acting complement C5 blocker that stops complement-driven inflammation in the kidneyIV infusion at a clinic every 8 weeks after a loading dose, weight-basedI CAN, Phase 3, 579 peoplePrimary endpoint: UPCR change at week 34 (interim); eGFR change at week 106 (final)
ClinicalTrials.gov
Met first primary endpoint: UPCR fell 46.6% vs 5.6% on placebo at week 34, a 43.4% reduction vs placebo (AstraZeneca press release, 2026-06-15, citing ERA Congress 2026)FDA decision anticipated in the fourth quarter of 2026 (priority review)
AstraZeneca press release, June 15, 2026
Roche (licensed from Ionis)
Phase 3as of October 1, 2026Antisense oligonucleotide that lowers complement factor B made by the liverShot under the skin once a month, designed for self-injectionIMAgINATION, Phase 3, 459 peoplePrimary endpoint: UPCR change at week 37
ClinicalTrials.gov
Met primary endpoint at a prespecified interim analysis; Roche has not released the size of the proteinuria reduction (Roche press release, 2026-09-23)No date announced
Roche media release, September 23, 2026
Novartis
Phase 3as of October 1, 2026Anti-APRIL antibody that lowers harmful IgA productionShot under the skin every 2 weeks (600 mg)BEYOND, Phase 3, 383 peoplePrimary endpoint: eGFR change from baseline at 104 weeks
ClinicalTrials.gov
No trial results published yetNovartis expects the BEYOND readout in the first half of 2027
Novartis Q2 2026 media release, July 21, 2026
Phase 3as of October 1, 2026Anti-CD38 antibody that removes the plasma cells making harmful IgAIV infusion at a clinicPREVAIL, Phase 3, about 454 people (planned)Primary endpoint: UPCR percent change at week 36
ClinicalTrials.gov
No trial results published yetNo date announced
ClinicalTrials.gov NCT06935357, updated September 30, 2026
Cost

Help paying for IgA nephropathy treatment

Drugmaker copay and free-drug programs, plus charity funds for the condition, checked every week.

Questions

IgA Nephropathy treatment questions people ask

What is the best treatment for IgA nephropathy?

No trial has compared the 6 approved drugs with each other, so there is no evidence-based ranking. Tarpeyo, Filspari and Fabhalta have shown on their labels that they slow the loss of kidney function over 2 years. Vanrafia, Trutakna and Voyxact were approved on protein reduction and are still confirming kidney benefit. The right choice depends on how much protein is in the urine, kidney function, whether a pill or an injection fits your life, and whether you can stop ACE inhibitors or ARBs, which Filspari requires.

Which IgA nephropathy drugs are pills?

Tarpeyo (capsule once a day for 9 months), Filspari (tablet once a day), Fabhalta (capsule twice a day) and Vanrafia (tablet once a day). Trutakna is a shot under the skin once a week and Voyxact a shot every 4 weeks, both self-injected at home.

What new IgA nephropathy drugs are coming?

As of October 2026, povetacicept has an FDA decision date of November 30, 2026, and Ultomiris (ravulizumab) has a decision expected in the fourth quarter of 2026 under priority review. Sefaxersen met its Phase 3 primary endpoint in September 2026 but Roche has not released the numbers. Zigakibart's Phase 3 readout is expected in the first half of 2027 and felzartamab is in Phase 3. The pipeline table on this page lists each one with its trial.

Which IgA nephropathy treatments have a boxed warning?

Filspari, for liver injury and harm to a fetus; Vanrafia, for harm to a fetus; and Fabhalta, for serious infections caused by encapsulated bacteria, which requires vaccination before starting. Tarpeyo, Trutakna and Voyxact have no boxed warning.

Does Tarpeyo cure IgA nephropathy?

No. Tarpeyo is a 9-month course of a targeted-release steroid that, in its trial, left kidney function 5.9 mL/min/1.73 m2 better than placebo at 2 years and lowered urine protein by 31% more than placebo at 9 months. The kidney function benefit held after the course ended, but the label notes it did not change the long-term rate of decline, and the disease itself is not removed.

Go deeper

More on IgA Nephropathy at Trial Friend

Sources

Where every number on this page comes from

Approved-drug facts are from the current FDA prescribing information on DailyMed, with the label's effective date. Investigational-drug facts are from ClinicalTrials.gov and the sources named in each row.

  1. Tarpeyo (budesonide delayed-release capsules) prescribing information, Calliditas Therapeutics, label dated Jan 2026. DailyMed. Pivotal trial: ClinicalTrials.gov
  2. Filspari (sparsentan) prescribing information, Travere Therapeutics, label dated Apr 2026. DailyMed. Pivotal trial: ClinicalTrials.gov
  3. Fabhalta (iptacopan) prescribing information, Novartis, label dated Jul 2026. DailyMed. Pivotal trial: ClinicalTrials.gov
  4. Vanrafia (atrasentan) prescribing information, Novartis, label dated Jun 2026. DailyMed. Pivotal trial: ClinicalTrials.gov
  5. Trutakna (atacicept-vymj) prescribing information, Vera Therapeutics, label dated Aug 2026. DailyMed. Pivotal trial: ClinicalTrials.gov
  6. Voyxact (sibeprenlimab-szsi) prescribing information, Otsuka, label dated Mar 2026. DailyMed. Pivotal trial: ClinicalTrials.gov
  7. povetacicept, Vertex Pharmaceuticals (Alpine Immune Sciences): ClinicalTrials.gov record; Vertex press release, June 1, 2026. Checked October 1, 2026.
  8. ravulizumab (Ultomiris), Alexion (AstraZeneca): ClinicalTrials.gov record; AstraZeneca press release, June 15, 2026. Checked October 1, 2026.
  9. sefaxersen, Roche (licensed from Ionis): ClinicalTrials.gov record; Roche media release, September 23, 2026. Checked October 1, 2026.
  10. zigakibart, Novartis: ClinicalTrials.gov record; Novartis Q2 2026 media release, July 21, 2026. Checked October 1, 2026.
  11. felzartamab, Biogen: ClinicalTrials.gov record; ClinicalTrials.gov NCT06935357, updated September 30, 2026. Checked October 1, 2026.

This page compares what the FDA labels and pivotal trials report. It is not medical advice, and no trial on this page compared these drugs with each other. Written and checked by Jason Hunter; the method is on the editorial standards page.