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Arginase 1 deficiency (hyperargininemia): US-approved treatments and how Gulf families can access them
A plain guide for families in the Gulf, checked against US FDA labels, Gulf drug registers and published medical research.
Reviewed by the Reserve Meds clinical operations team on 17 October 2026.
Arginase 1 deficiency: the short answer
For arginase 1 deficiency, the US FDA has approved one medicine covered on this page, for a specific group of patients: Loargys. Loargys is already on at least one Gulf list, so start by asking your hospital about local supply. Where a medicine is not registered in your country, the treating hospital can ask the national regulator for permission to import it for one named patient. Reserve Meds is a digital health company that helps families and hospitals with that process. We do not diagnose or prescribe.
- US FDA-approved medicines on this page: Loargys.
- Gulf registration (checked 17 October 2026): see each medicine below.
- Legal route: Local supply where listed; otherwise a named-patient import request filed by the treating hospital.
- Price: Quote on request.
What is arginase 1 deficiency?
Arginase deficiency is an inherited disorder in which the amino acid arginine and ammonia build up gradually in the blood. It usually becomes evident by about age 3, most often as stiffness in the legs (spasticity). Other signs can include slow growth, developmental delay and loss of skills, seizures, tremor and problems with balance. High-protein meals, illness or fasting can make ammonia rise faster.[1]
It belongs to the urea cycle disorders, is caused by variants in the ARG1 gene and is inherited in an autosomal recessive pattern. It is very rare, estimated at once in every 300,000 to 1,000,000 people.[1]
Arginase 1 deficiency in the Gulf
A 2018 report from Bahrain described a 14-year-old girl whose arginase deficiency was diagnosed late, after neurological complications had developed. The authors, from the Arabian Gulf University, King Hamad University Hospital and Kuwait University, said these complications could have been avoided with newborn screening and called for a national screening policy in Bahrain.[2]
On 17 October 2026, Loargys was listed in the Abu Dhabi Department of Health drug code list and was not found in the SFDA drugs list.[3, 4]
US FDA-approved medicines for arginase 1 deficiency
Each medicine below is approved in the US for a specific group of patients. The wording follows the current US label. Your specialist decides whether any of them is right for the patient.
- Loargys (pegzilarginase-nbln)
FDA-approved for high blood arginine in adults and children aged 2 and older with arginase 1 deficiency, together with a protein-restricted diet. Treatment starts in a healthcare setting that can manage allergic reactions. Approved under accelerated approval, based on lower plasma arginine.[5, 6]
US FDA approval: 23 February 2026. Gulf registers: Saudi Arabia: not found in the SFDA drugs list. Abu Dhabi: listed in the Abu Dhabi DoH drug code list. Checked 17 October 2026. Kuwait, Qatar and Oman: no public register checked.[4, 3]
How families in the Gulf can access these medicines
If the medicine is listed in your country. Ask your specialist and the hospital pharmacy about local supply first. A listing does not mean every hospital stocks the medicine, but it is usually the fastest route, and you may not need us.
If it is not registered. The usual legal route is a named-patient request: the treating hospital, on your specialist's written request, asks the national regulator for permission to import the medicine for one patient, using the US FDA approval as the reference. In Saudi Arabia the SFDA Special Access Program guidance covers these requests; in Bahrain, NHRA Circular 41 of 2020 sets the procedure. Other Gulf countries have their own procedures, which the hospital pharmacy confirms.[7, 8] Once approval is in place, Reserve Meds arranges supply through a US-licensed pharmaceutical wholesale partner to the hospital pharmacy.
Who does what
- Your treating specialist decides whether a medicine is right for the patient and writes the letter.
- The hospital checks local supply, files any import request, and gives the treatment safely.
- The national regulator decides whether to approve the import of a medicine that is not registered.
- The manufacturer decides where its medicine can be supplied, especially for cell and gene therapies.
- Reserve Meds helps organize records, coordinates US supply through our wholesale partner, shipping and updates to your family. We do not give medical advice.
Documents you will usually need
- A letter from the treating specialist with the diagnosis, past treatments and why this medicine is being considered
- Reports that confirm the diagnosis, such as genetic, pathology or laboratory results, translated into English where needed
- Recent clinic notes and a list of current medicines
- For a hospital import request: the prescription, the hospital's request form and the written consent of the patient or guardian
- Proof of the US FDA approval and the US prescribing information (we can supply these)
We give you a written timeline estimate once we see the hospital file. The regulator, the treatment center and the manufacturer set their own timelines.
What treatment costs
Quote on request. Your total cost depends on the medicine, the dose, shipping, import steps and coordination. Your coordination fee is quoted in writing for your case before you commit. No hidden charges.
How Reserve Meds helps
Reserve Meds is a digital health company. Medicines are supplied through a US-licensed pharmaceutical wholesale partner. We help your doctor and hospital prepare the file, arrange US supply and temperature-controlled shipping once approval is in place, and keep your family updated. We coordinate access to FDA-approved medicines only. Investigational medicines are only available through a manufacturer's expanded-access program requested by the treating physician; we can explain that route, but we do not supply them.
Ask us about treatment for arginase 1 deficiency
Tell us the medicine, the country, and how to reach you. We reply within one business day. On WhatsApp we usually reply the same day.
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Your coordination fee is quoted in writing for your case before you commit. No hidden charges.
Frequently asked questions
Is there an FDA-approved treatment for arginase 1 deficiency?
Yes. The medicine on this page has US FDA approval for a specific group of patients: Loargys. The exact conditions are in the US label and are summarized above. Your specialist decides whether it fits.
Is Loargys available in Saudi Arabia or the UAE?
Saudi Arabia: not found in the SFDA drugs list. Abu Dhabi: listed in the Abu Dhabi DoH drug code list. Checked 17 October 2026. Kuwait, Qatar and Oman: no public register checked. A listing in Abu Dhabi does not show federal UAE status, which we could not verify.
How can a family in the Gulf get Loargys?
Ask the treating hospital about local supply first. If it is not available, the hospital can file a named-patient import request with the national regulator on your specialist's written request. Once approved, we arrange US supply to the hospital pharmacy.
How much does treatment cost?
Quote on request. Your total cost, including the medicine, shipping, import steps and coordination, is quoted in writing for your case before you commit. No hidden charges.
Does Reserve Meds diagnose or prescribe?
No. Reserve Meds is a digital health company. Medicines are supplied through a US-licensed pharmaceutical wholesale partner. We do not diagnose, prescribe or decide what a regulator approves. Your specialist and hospital make the medical decisions.
Does Loargys replace the special diet?
No. The US label says Loargys is used together with dietary protein restriction. Treatment starts in a healthcare setting that can manage allergic reactions.
Sources for the last answer: [6]
Sources
Checked on 17 October 2026. Labels, registers and regulator rules change. Your hospital pharmacy confirms the current position before filing.
- MedlinePlus Genetics: Arginase deficiency
- Bakhiet M, et al. Neurological complications owing to lately diagnosed hyperargininemia: the role of national neonatal screening in the Kingdom of Bahrain. Medicine. 2018 (PubMed 29768370)
- Department of Health Abu Dhabi: drug code list Drugs.xlsx (release 26 September 2026, effective 2 October 2026)
- SFDA: Drugs List, public register (all 9,173 entries checked by brand and generic name on 17 October 2026)
- FDA: Novel Drug Approvals for 2026
- DailyMed: LOARGYS (pegzilarginase-nbln) US prescribing information (label version 23 February 2026)
- SFDA: Special Access Program (SAP) guidance, version 1.0
- NHRA Bahrain: Circular No. (41) of 2020, procedures for importing non-registered medicines and pharmaceutical products
Related
- Urea cycle disorders
- Other rare metabolic diseases
- Named-patient access in the Gulf, explained
- Answers to common access questions
- Cross-border disclosures
- اقرأ هذه الصفحة بالعربية
This page is general health information, not medical advice. It does not replace a consultation with your doctor.