FIP Antivirals: the History of Feline Treatment

Complete history of FIP treatment: from pre-2017 palliatives to GS-441524, mefloquine and nirmatrelvir. Comparative table of clinical studies. Written by specialist veterinarians.

By Vicky Vives Moya & Esther Garrido Cervera FIP antiviralsmefloquineFIP treatment historyDr. PedersennirmatrelvirFIP studies

Until 2017, a FIP diagnosis was a death sentence. The available treatments were exclusively palliative and cats died within weeks. Today, thanks to antivirals, 93% of treated cats make a full recovery. This is the story of how that change happened, and a detailed guide to all available antivirals: including those without their own page on this site.

Authorship note: This article was written by Vicky Vives Moya, Licenced in Veterinary Medicine specialising in Feline Medicine (Cert. Ophthalmology, AVEPA, GEMFE, iCatCare member), and Esther Garrido Cervera, Licenced in Veterinary Medicine. Last reviewed: November 2025. The authors have no conflict of interest with antiviral manufacturers or commercial suppliers.

For detailed information on the main antivirals, see our dedicated guides: GS-441524 · Molnupiravir.


1. Before antivirals: the pre-2017 landscape

For decades, FIP treatment was limited to relieving symptoms with no real impact on survival. The drugs used fell into three strategies:

CategoryDrugsGoal
CorticosteroidsPrednisolone, DexamethasoneAnti-inflammatory and immunosuppressant
Alkylating agentsCyclophosphamideImmunosuppressant
Cytokine inhibitorsPentoxifyllineAnti-vasculitis
Non-specific antiviralsDoxycycline, Cyclosporin ALimited in-vitro antiviral activity
ImmunostimulantsFeline recombinant omega interferon (rfIFN-ω), PPIImmune stimulation
ExperimentalItraconazole, stem cellsNo consistent efficacy

The outcome was always the same: temporary relief of days or weeks, with no change to the fatal prognosis. Cyclosporin A showed some anti-coronavirus activity by blocking non-structural protein Nsp1, and recombinant omega interferon was used in monotherapy or combined with glucocorticoids, but neither altered disease progression.

Polyprenyl immunostimulant (PPI) produced some documented successes in non-effusive FIP, but without consistent reproducibility.


2. Dr. Niels Pedersen and the antiviral revolution (2017–2019)

Dr. Niels Pedersen, veterinarian and professor emeritus at the University of California, Davis, has been studying feline infectious diseases for decades. His work was decisive:

  • 1970s: start of his research into FIP
  • 2008: comprehensive review of all FIP scientific literature published to that date
  • 2017: first study with a protease inhibitor showing promising results in cats with FIP
  • 2019: publication of GS-441524 data that forever changed the disease prognosis

His publications opened the door to what we know today: FIP is curable.


3. GS-441524 and Remdesivir: the gold standard

GS-441524 and remdesivir are nucleotide analogues that inhibit the RNA polymerase of feline coronavirus, stopping viral replication. GS-441524 is the active form of remdesivir.

Since 2019, thousands of treated cases worldwide confirm a 93% cure rate. In 2023, the WSAVA included them on its list of essential medicines for dogs and cats.

Full guide on our dedicated page: GS-441524 for FIP

4. Molnupiravir: alternative for resistant cases

Molnupiravir (EIDD-2801, marketed as Lagevrio® by Merck) acts by inducing errors in viral RNA until the virus stops replicating. It has shown efficacy in FIP including neurological and ocular forms.

International Cat Care mentions it for cases of GS-441524 therapeutic failure.

Full guide: Molnupiravir for FIP


5. Mefloquine: the economical option

Mechanism of action

Mefloquine is a human antimalarial (Lariam®) used against chloroquine-resistant Plasmodium falciparum. Its activity against feline coronavirus was discovered following COVID-19 research.

In vitro, it reduces FIP viral load in feline renal cells (Crandell) without cytotoxic effect, inhibiting viral replication.

Scientific evidence

2013 study (chloroquine): Chloroquine, from the same pharmacological family, demonstrated an inhibitory effect against FIP virus replication and anti-inflammatory activity in vitro. Experimentally infected cats treated with chloroquine showed better clinical outcomes.

2020 study (mefloquine: in vivo pharmacokinetics): Study that determined the efficacy of current doses, described haematological and biochemical changes during treatment and established the safety profile in clinically normal cats.

Dosage

ParameterValue
Standard dose62.5 mg, 2–3 times per week
DurationUp to completing 84 days
RouteOral

Use in combination

Mefloquine is used primarily as a supplement to GS-441524, potentiating antiviral effects, or as a more economical alternative in the International Cat Care protocol when access to GS-441524 is limited.

Adverse effects

  • Vomiting (administer with food to minimise)
  • Dermatopathies (skin reactions)
  • Elevated SDMA (renal function marker)

6. Nirmatrelvir: current research

The journal Veterinary Sciences published an article in 2023 comparing the in-vitro efficacy of different antivirals against FIP, with promising results for nirmatrelvir.

Nirmatrelvir is marketed together with ritonavir under the name Paxlovid® (Pfizer), for exclusive human use against COVID-19. According to personal communication from Dr. Richard Malik, it has been used in cats refractory to other treatments.

Reported protocol: 75 mg nirmatrelvir + 25 mg ritonavir every 12 hours, oral route.

This dosage is based on individual cases under specialist supervision. It is not approved for veterinary use and requires a special prescription. Formal clinical studies are needed to establish definitive protocols.


7. Comparative table of clinical studies

StudyCasesSurvivalRelapse rate
Pedersen 2019 (original GS-441524)3177%30.8%
GTA-AVEPA 2023: Spain8977.5%7.2%
International Cat Care 202330784.4%10.8%
Vives Moya 2025500+88.1%8%

Clear trend: the most recent studies, with optimised protocols and higher doses, show increasing survival rates and declining relapse rates. The doses used in Pedersen’s original study (2 mg/kg) were far lower than current protocols (6–10 mg/kg depending on FIP form).


8. Antiviral selection algorithm

Clinical situationFirst line
Effusive FIP without complicationsGS-441524 or remdesivir
Non-effusive FIPGS-441524 or remdesivir
Neurological FIPHigh-dose GS-441524 (min. 10 mg/kg injectable)
Ocular FIPGS-441524 or remdesivir
GS-441524 resistanceIncrease the dose and consider molnupiravir
Post-treatment relapseRestart GS-441524 (higher dose)
Economic limitationMefloquine + GS-441524 (reduced dose)
Failure with multiple antiviralsNirmatrelvir (experimental use, specialist)

9. Treatment monitoring

Dr. Pedersen established the monitoring criteria in 2019 that remain the standard:

  • Clinical evaluation: weekly for the first 2–4 weeks, then fortnightly
  • Complete blood count: every 2–4 weeks
  • Serum biochemistry: total protein, albumin, globulins, bilirubin, ALT, creatinine
  • Body weight: weekly
  • Temperature: daily at home during the first weeks
  • Ultrasound: if effusion present, to monitor its resolution

Indicators of good response:

  • Resolution of fever within the first 24–48 hours
  • Improvement of appetite and activity within 3–7 days
  • Decrease in globulins and increase in albumin
  • Resolution of effusion within 2–4 weeks

10. Organisations and reference sources


Medical disclaimer: This guide is informational and educational, based on peer-reviewed scientific literature. It does not replace professional veterinary consultation, diagnosis or treatment. FIP treatment with antivirals must always be carried out under veterinary supervision. The authors have received no financial compensation and declare no conflict of interest.

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