Recovery in 4 to 8 Weeks
97% Success Rate
Zero Injections, easy at home treatment
Substantially higher intrinsic antiviral potency than Molnupiravir EIDD-2801
Rapid reduction of FCV replication
long-term management of calicivirus

تم التحقق منه علميًا
وقد أظهرت الدراسات السريرية التي تمت مراجعتها من قبل النظراء في الولايات المتحدة وأوروبا أن EIDD-1931 الذي تقدمه MolnuFIP ™ يتمتع بمعدل نجاح علاجي بنسبة 97٪.

Professional
Treatment
Advice
نحن هنا لخدمتكم على مدار الساعة طوال أيام الأسبوع! تواصلوا معنا عبر البريد الإلكتروني، أو الدردشة المباشرة، أو واتساب في أي وقت للبدء.

توصيل سريع
لدينا مستودعات محلية في الدول التي نقدم فيها خدمة معالجة FIP. نضمن توصيلًا موثوقًا لكل طلب.

No
Injections
يمكن تناول Molnufip™ EIDD - 1931 في كبسولات هلامية ناعمة بسهولة في المنزل. مرتين في اليوم. بفاصل 12 ساعة.
"EIDD-1931 غير مناسب لجميع حالات FIP. يجب على القطط التي تعاني من أعراض FIP العصبية والعينية، ومشاكل الشهية والجهاز الهضمي، وأمراض الكلى والكبد الموجودة مسبقًا، أن تبدأ علاج FIP بحقن GS-441524 لمدة 2 - 4 أسابيع قبل التبديل إلى EIDD-1931.
FAQs
CaliciX™ Max is a high-strength systemic antiviral capsule formulated for cats suffering from severe, refractory, or high-viral-load feline calicivirus (FCV) disease, where standard-dose therapy may be insufficient.
CaliciX™ Max delivers 30 mg of EIDD-1931 per capsule, enabling veterinarians to achieve higher systemic antiviral suppression with fewer capsules compared to CaliciX™.
It is intended for step-up therapy in advanced, severe, or poorly responsive feline calicivirus (FCV) cases.
CaliciX™ Max may be considered under veterinary supervision when a cat has:
Severe oral or oropharyngeal disease
Refractory FCGS or post-extraction stomatitis
High systemic viral burden
Poor response to 2-4mg/kg dosing
Larger body weight requiring higher per-dose exposure
CaliciX™ Max is formulated to support cats with severe FCV-associated disease, including:
Severe feline chronic gingivostomatitis (FCGS)
Caudal stomatitis with extensive inflammation
Deep lingual ulceration (viral glossitis)
Multifocal oral ulceration
Virulent systemic feline calicivirus (VS-FCV)
Yes, CaliciX™ Max is designed for veterinarian-directed use in such severe presentations, alongside intensive supportive care.
No. CaliciX™ Max is not an antibiotic. It is a direct-acting antiviral designed to suppress FCV viral replication. Antibiotics may still be used separately to manage secondary bacterial infections when indicated.
EIDD-1931 interferes with viral RNA replication by inducing lethal mutagenesis in RNA viruses. This mechanism:
Does not rely on viral proteases
Has a high genetic barrier to resistance
Works independently of host immune status
CaliciX™ Max may be used as part of an extended management plan in cats with chronic or refractory feline calicivirus (FCV) where ongoing antiviral control is clinically indicated.
Treatment duration, dose adjustments, and monitoring should always be determined by a licensed veterinarian based on the individual patient’s response and overall health status.
No. CaliciX™ Max is intended to be part of a comprehensive veterinary treatment plan, which may include dental procedures, pain control, nutritional support, and other therapies as needed.
No. CaliciX™ Max is not the same as human molnupiravir.
It contains EIDD-1931, the active antiviral metabolite of molnupiravir—the form that directly exerts antiviral activity. Published research indicates that EIDD-1931 demonstrates significantly higher antiviral potency than molnupiravir, which is a prodrug requiring metabolic conversion.
CaliciX™ Max is formulated specifically for veterinary use in cats, with dosing, capsule size, and clinical intent designed for feline patients rather than humans.
It may not be suitable for:
Pregnant or breeding cats
Cats with significant hepatic or renal disease
CaliciX™ Max is intended for veterinary-supervised use only.
The 30 mg strength allows veterinarians to:
Achieve higher antiviral exposure
Reduce capsule burden in large or severe cases
Improve dosing accuracy and compliance
This makes it suitable for advanced or high-risk FCV disease.





