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Updated: January 25, 2026

What Is Glutamine (Endari)? Uses, Dosage, and What You Need to Know in 2026

Author

Peter Daggett

Peter Daggett

What is Glutamine Endari - information guide

Glutamine (Endari) is the first FDA-approved treatment for sickle cell disease in nearly 20 years. Learn what it is, how it's used, the correct dosage, and key facts for 2026.

Glutamine, sold under the brand name Endari, is an FDA-approved prescription medication for sickle cell disease (SCD). While glutamine is an amino acid your body naturally produces and you get from food, pharmaceutical-grade prescription Glutamine is specifically formulated to reduce the serious complications of sickle cell disease — a role that regular food or over-the-counter supplements cannot reliably fill.

This guide covers everything you need to know about Glutamine (Endari) — what it is, what it treats, how to take it, and key facts for 2026.

What Is Glutamine (Endari)?

Glutamine is an amino acid — one of the 20 building blocks of protein. It's the most abundant amino acid in the human body and plays important roles in immune function, gut health, and cellular energy production. While the body normally produces enough glutamine, certain medical conditions — including sickle cell disease — create an increased demand that the body cannot meet on its own.

Prescription Glutamine (Endari) is pharmaceutical-grade L-glutamine oral powder, formulated specifically for medical use. It comes in precisely measured 5-gram foil packets and is available only by prescription through specialty pharmacies.

What Is Glutamine Approved to Treat?

The FDA approved Glutamine (Endari) in July 2017 for one specific indication:

Reducing the acute complications of sickle cell disease in adults and pediatric patients 5 years of age and older.

This was a landmark approval. It was the first new treatment for sickle cell disease in nearly 20 years — and the first treatment ever approved specifically for children with SCD. Prior to Endari, hydroxyurea (approved in 1998) was the only FDA-approved oral medication for SCD.

Acute complications of SCD that Glutamine helps reduce include:

Vaso-occlusive crises (VOCs) — painful episodes caused by sickled red blood cells blocking small blood vessels

Hospitalizations due to sickle cell pain crises

Acute chest syndrome episodes (fewer episodes were seen in the Glutamine group in trials)

What Forms Does Glutamine Come In?

Prescription Glutamine for sickle cell disease comes in one form: oral powder in individual 5-gram foil packets. Each packet contains white crystalline powder that must be mixed with a liquid or soft food before taking.

It is NOT available as a tablet, capsule, liquid, or injection for this indication. The only other forms of L-glutamine available (OTC supplements) are not FDA-approved for sickle cell disease.

Glutamine Dosage: How Much Do You Take?

The dose of Glutamine is based on your body weight. The recommended dose is 0.3 grams per kilogram of body weight, taken twice daily:

Under 30 kg (66 lbs): 5 grams (1 packet) twice daily = 10 g/day

30 to 65 kg (66–143 lbs): 10 grams (2 packets) twice daily = 20 g/day

Over 65 kg (143 lbs): 15 grams (3 packets) twice daily = 30 g/day (maximum dose)

These doses are significantly higher than any OTC glutamine supplement provides — which is one reason why supplements cannot substitute for prescription Endari.

How to Take Glutamine (Endari)

Measure or take the correct number of 5-gram packets for your dose

Pour the powder into 8 oz (240 mL) of a cold or room-temperature beverage (water, milk, apple juice) OR into 4–6 oz of cold soft food (yogurt, applesauce)

Stir to mix (complete dissolution is not required)

Drink or eat it immediately — do not prepare in advance

⚠️ Important: Do NOT mix with hot food or liquid — heat can degrade the medication

Does Glutamine Work? What the Clinical Evidence Shows

The FDA approval was based on a Phase 3 randomized, double-blind, placebo-controlled trial involving 230 patients (ages 5–58) with sickle cell anemia or sickle β0-thalassemia. Results after 48 weeks:

Median number of pain crises: 3 in the Glutamine group vs. 4 in placebo (statistically significant, p=0.005)

Hospitalizations: 33% fewer in the Glutamine group compared to placebo

Acute chest syndrome: fewer episodes in the Glutamine group

Key Facts at a Glance

Brand name: Endari (generic available since July 2024)

Drug class: Amino acid / antioxidant precursor

FDA approval: July 2017, for ages 5+

Controlled substance: No

Pharmacy type: Specialty pharmacy only

Cash price: ~$3,200+ per 30-day supply retail; ~$1,013 with GoodRx coupon

Learn more about how Glutamine works at a molecular level. Ready to find Glutamine at a pharmacy near you? Try medfinder.

Frequently Asked Questions

Glutamine (Endari) is FDA-approved to reduce the acute complications of sickle cell disease — specifically painful vaso-occlusive crises and hospitalizations — in adults and children ages 5 and older. It is not approved for any other indication.

No. While both contain the amino acid L-glutamine, prescription Endari is pharmaceutical-grade, precisely dosed, and formulated specifically for sickle cell disease. OTC supplements come in much lower doses and are not FDA-approved for SCD. Clinical trials used doses up to 30g/day — far more than most supplements provide.

Clinical benefits were measured over a 48-week trial, and effects are cumulative. Glutamine is not a rescue medication for acute pain crises — it's a preventive treatment taken daily to reduce the frequency and severity of future crises. It may take weeks to months of consistent use before the full benefit is apparent.

No. Glutamine is a continuous preventive treatment, not something you take only during a crisis. Stopping and starting could reduce its effectiveness. If you want to stop taking Glutamine, talk to your hematologist first — they can help you taper off safely and evaluate your overall SCD management plan.

The FDA approved Endari (L-glutamine oral powder) in July 2017 for reducing acute complications of sickle cell disease in patients ages 5 and older. It was the second drug approved for SCD and the first new SCD treatment in nearly 20 years. The first FDA-approved generic version launched in July 2024.

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