Tretten vs Corifact for Factor XIII: What's the Difference?
At a Glance
The primary difference is that Tretten is a lab-made, synthetic treatment that only treats Subunit A deficiency, while Corifact is derived from human blood plasma and can treat both Subunit A and Subunit B Factor XIII deficiencies.
In this answer
5 sections
Getting diagnosed with a rare bleeding disorder like Factor XIII (Factor 13) deficiency can feel overwhelming, especially when faced with new medical terminology and treatment decisions. If you need replacement therapy, your doctor may recommend treatment with either Tretten or Corifact.
The main difference between these two treatments lies in how they are made and which parts of the Factor XIII protein they contain. Tretten is a lab-made (synthetic) treatment that replaces only the “A” part of the Factor XIII protein [1], while Corifact is made from human blood plasma and replaces both the “A” and “B” parts of the protein [2]. Because of these differences, the specific type of Factor XIII deficiency you have determines which medication is a safe and effective option for you.
Understanding Your Diagnosis: Subunit A vs. Subunit B
Factor XIII is normally found in your blood as a complex made of two parts: Subunit A and Subunit B [2][3]. Subunit A is the “active worker” that helps form strong blood clots, while Subunit B acts as a “carrier protein” that stabilizes Subunit A and helps it move safely through your bloodstream [4][5].
When you are diagnosed with Factor XIII deficiency, specialized blood work or genetic testing is typically done as a standard part of your diagnosis to show whether you are missing Subunit A or Subunit B. Most people with this condition have a deficiency in Subunit A [6][1]. Knowing your specific subtype is critical because it dictates which treatment your body can use.
Tretten: The Recombinant Option
Tretten is a recombinant factor product, which means it is artificially created in a laboratory rather than being drawn from human blood donors [3][1]. It is specifically engineered to provide only Subunit A [1][2].
Because it lacks Subunit B entirely, Tretten is only approved and effective for patients who have Subunit A deficiency [1][3]. If you have a Subunit B deficiency, your body would not have the carrier protein needed to stabilize the synthetic Subunit A provided by Tretten, making it an inappropriate treatment choice. Since Tretten is lab-made, it carries zero risk of transmitting human blood-borne viruses [3].
Corifact: The Plasma-Derived Option
Corifact is a plasma-derived concentrate. This means it is purified from the pooled blood plasma of healthy human donors. The manufacturing process includes strict purification and viral inactivation steps to heavily reduce the risk of transmitting infections [3][7]. However, because it comes from human blood, a theoretical risk of infection remains.
Unlike Tretten, Corifact contains both Subunit A and Subunit B just as they appear naturally in human blood [2][1]. Because it provides both parts of the protein, Corifact can be used to treat patients with either Subunit A or Subunit B deficiency [7][2].
How Treatment Looks: Administration and Safety
Both Tretten and Corifact are given directly into the bloodstream as an intravenous (IV) infusion [8][1]. They are commonly prescribed for prophylaxis (routine prevention) to stop bleeds before they start, which often involves an infusion around every 28 days, depending on how your body processes the medication [8][1]. They can also be used to manage bleeding around the time of surgery [8][9]. Over time, many patients or their caregivers learn to safely perform these infusions at home.
Overall, both medications are highly effective and generally well-tolerated, but there are potential side effects to be aware of:
- Allergic reactions: As with any infused protein, there is a risk of allergic reactions, ranging from mild skin rashes to more severe responses during the infusion [10].
- Inhibitors: In very rare cases, your immune system might mistake the replacement factor as a foreign threat and develop “inhibitors” (antibodies) that stop the medication from working [11][12].
- Blood clots: Since these medications help your blood clot, there is a theoretical risk of blood clots (thrombosis), especially if you have other risk factors [13].
Summary of Differences
- Composition: Tretten is lab-made (synthetic) [3]. Corifact is derived from human blood plasma [7].
- Infection Risk: Tretten carries no human viral risk [3]. Corifact carries a very small, theoretical risk despite rigorous safety steps [7].
- Subunits included: Tretten contains only Subunit A [1]. Corifact contains both Subunit A and Subunit B [2].
- Who can take it: Tretten is exclusively for people with Subunit A deficiency [1]. Corifact can be taken by people with either Subunit A or Subunit B deficiency [7][2].
Common questions in this guide
What is the main difference between Tretten and Corifact?
Can I use Tretten if I have a Subunit B deficiency?
Is there a risk of getting a virus from these Factor XIII treatments?
How are Tretten and Corifact administered?
Questions for Your Doctor
5 questions
- •Which specific subunit (A or B) am I missing, and how does that affect my treatment choices?
- •What are the warning signs of an allergic reaction or an inhibitor developing that I should watch for during or after my infusions?
- •Will I be taking this medication for routine prevention (prophylaxis), or only when I have an active bleed or upcoming surgery?
- •Is it possible for me or a family member to learn how to safely administer these IV infusions at home?
- •Do I have any other medical conditions or risk factors that might increase my risk of a blood clot while on this therapy?
Questions for You
3 questions
- •How comfortable do I feel receiving a medication derived from human blood plasma versus a synthetic, lab-made product?
- •What is my current ability to manage regular IV infusions, and how might a routine monthly treatment schedule fit into my daily life?
- •Have I ever had a negative reaction to an infused or injected medication or blood product in the past?
References
References (13)
- 1
Safety and effectiveness of recombinant factor XIII-A2 in congenital factor XIII deficiency: Real-world evidence.
Poulsen LH, Kerlin BA, Castaman G, et al.
Research and practice in thrombosis and haemostasis 2022; (6(2)):e12628 doi:10.1002/rth2.12628.
PMID: 35243202 - 2
Factor XIII topology: organization of B subunits and changes with activation studied with single-molecule atomic force microscopy.
Protopopova AD, Ramirez A, Klinov DV, et al.
Journal of thrombosis and haemostasis : JTH 2019; (17(5)):737-748 doi:10.1111/jth.14412.
PMID: 30773828 - 3
Successful perinatal management of a woman with congenital factor XIII deficiency using recombinant factor XIII: A case report and literature review.
Ito Y, Tsuji S, Kasahara M, et al.
The journal of obstetrics and gynaecology research 2024; (50(2)):262-265 doi:10.1111/jog.15819.
PMID: 37875278 - 4
Exploring the function of factor XIII free B subunit: Interactions with complement factors and a novel approach to identify potential binding partners.
Li B, Bechtler C, Jenny L, et al.
Research and practice in thrombosis and haemostasis 2022; (6(5)):e12766 doi:10.1002/rth2.12766.
PMID: 35873217 - 5
Reciprocal stabilization of coagulation factor XIII-A and -B subunits is a determinant of plasma FXIII concentration.
Byrnes JR, Lee T, Sharaby S, et al.
Blood 2024; (143(5)):444-455 doi:10.1182/blood.2023022042.
PMID: 37883802 - 6
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.
Ivaškevičius V, Biswas A, Garly ML, Oldenburg J
Haemophilia : the official journal of the World Federation of Hemophilia 2017; (23(3)):e194-e203 doi:10.1111/hae.13233.
PMID: 28520207 - 7
Massive recurrent post-tonsillectomy bleedings revealing a transient factor XIII deficiency in a 10-year-old boy. A case report.
Jankovic M, Choucair ML, Hallak B, et al.
International journal of pediatrics & adolescent medicine 2019; (6(2)):55-57 doi:10.1016/j.ijpam.2019.05.006.
PMID: 31388547 - 8
Use of Catridecacog in a patient with severe Factor XIII deficiency undergoing surgery.
Sottilotta G, Luise F, Oriana V, et al.
Hematology reports 2019; (11(1)):7912 doi:10.4081/hr.2019.7912.
PMID: 30915205 - 9
Treatment with Recombinant Factor XIII (Tretten) in a Pregnant Woman with Factor XIII Deficiency.
Abdel-Samad N
The American journal of case reports 2017; (18()):436-439 doi:10.12659/ajcr.901502.
PMID: 28432284 - 10
The pharmacokinetics of recombinant FXIII (catridecacog) from the MENTORTM2 trial to a real-world study: a head-to-head comparison.
Pasca S, PierGiorgio C, Pea F,
Journal of thrombosis and thrombolysis 2022; (54(4)):593-596 doi:10.1007/s11239-022-02700-x.
PMID: 36094687 - 11
Alloantibody developed in a factor XIII A subunit deficient patient during substitution therapy; characterization of the antibody.
Pénzes K, Vezina C, Bereczky Z, et al.
Haemophilia : the official journal of the World Federation of Hemophilia 2016; (22(2)):268-275 doi:10.1111/hae.12786.
PMID: 26249653 - 12
Inhibitors in Patients with Congenital Bleeding Disorders Other Than Hemophilia.
Franchini M, Marano G, Mengoli C, et al.
Seminars in thrombosis and hemostasis 2018; (44(6)):595-603 doi:10.1055/s-0037-1607441.
PMID: 29165739 - 13
Developing the First Recombinant Factor XIII for Congenital Factor XIII Deficiency: Clinical Challenges and Successes.
Carcao M, Fukutake K, Inbal A, et al.
Seminars in thrombosis and hemostasis 2017; (43(1)):59-68 doi:10.1055/s-0036-1585076.
PMID: 27556350
This page explains the differences between Tretten and Corifact for educational purposes only. Always consult your hematologist or healthcare provider to determine the safest treatment plan for your specific type of Factor XIII deficiency.
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