Alizin

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Alizin

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Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Alizin

Quick Facts: Alizin

Property Description
Active ingredient Aglepristone
Form Sterile solution for injection
Pharmacological class Antiprogestogen (Progesterone Receptor Modulator)
Target species Bitches (dogs) and Queens (cats)
Origin Synthetic steroid

What is Alizin?

Alizin is a prescription-only veterinary medicinal product defined by its single active substance, Aglepristone, and is used exclusively in animal health, specifically for bitches and queens. The compound is a potent, manufactured synthetic steroid belonging to the antiprogestogen pharmacological class. Alizin is unique in its dedicated focus as a veterinary therapeutic agent for companion animals, differentiating it from human-specific progesterone modulators.


What Type of Veterinary Medicine is Alizin?

Alizin is formally classified as an antiprogestogen, a category of drugs that specifically counteracts the biological actions of the natural hormone progesterone by binding to its receptors. Aglepristone is recognized for its function as a competitive antagonist, meaning it physically blocks progesterone from reaching its designated cellular receptors, thereby initiating its pharmacological effect. This specific mechanism of action is utilized for managing certain reproductive states in animals.


Aglepristone: Composition and Physical Form

The functional component of Alizin is the active ingredient, Aglepristone, which is delivered as a sterile solution for injection. This formulation is a clear, yellow, non-aqueous liquid, utilizing an oily vehicle composed of refined arachis oil combined with anhydrous ethanol as excipients. Designed exclusively for delivery via subcutaneous injection, this specific oily composition facilitates a slow, sustained absorption of Aglepristone from the injection site, which is a key differentiator from standard aqueous preparations and enhances its therapeutic window.


General Purpose of a Progesterone Antagonist

The general therapeutic purpose of Alizin is intrinsically linked to its ability to counteract progesterone, the essential hormone responsible for maintaining the internal conditions necessary for gestation. By having Aglepristone act as a powerful receptor blocker, Alizin effectively interrupts the hormonal signals that perpetuate pregnancy in female animals. This resultant inhibition of progesterone action makes the drug a targeted agent for managing specific reproductive conditions by disrupting the underlying physiological processes that support the reproductive phase.

Regulatory References

  1. Vet. Med. Dir., SPC Summary

What side effects are possible with Alizin?

Possible Side Effects and Safety Information

The safety profile for Alizin (Aglepristone) is defined by classifications provided in regulatory documents, which group possible adverse reactions by frequency and physiological system. The most frequently observed reactions are related to the administration of the sterile solution.

Frequency-Classified Adverse Reactions

Classification Examples of Documented Reactions
Very Common (ge 1/10) Pain during or shortly after injection, local inflammation, swelling, or oedema at the injection site.
Common (1/100 to 1/10) Lethargy, anorexia, vomiting, diarrhoea, and a bloody or mucoid uterine discharge.
Rare (1/10,000 to 1/1,000) Hypersensitivity reactions, severe or persistent local reactions at the injection site, and lack of efficacy leading to complications.

System-Organ-Class Safety Groupings

The documented adverse effects primarily fall into three system-organ classes: General disorders and administration site conditions (covering pain and local swelling), Gastrointestinal disorders (including anorexia and vomiting), and Blood and lymphatic system disorders (transient changes in haematological parameters).

Safety-Related Contraindications and Limitations

The official labeling establishes clear limitations on the use of Alizin. The medicine is formally contraindicated in animals with known impaired hepatic or renal function due to metabolic concerns. It should also not be used in animals with pre-existing conditions such as hypoadrenocorticism (Addison’s disease) or in cases of known hypersensitivity to Aglepristone or its excipient, refined arachis oil. Local reactions at the injection site typically resolve within 28 days, but rare, severe inflammation may persist for several months.

Overdose and Emergency Response

The official regulatory documents detail the overdose profile of Alizin, which is primarily focused on the potential for localized effects in the target species and the distinct hazard posed by accidental human exposure.

In the target species (bitches), administration at three times the recommended therapeutic dose showed no adverse systemic effects. Overdose manifestations observed in controlled studies were restricted to local inflammatory reactions at the injection site. These local reactions were attributed to the larger volumes of the product, consistent with its formulation as an oil-based sterile solution. Management in these scenarios is limited to general symptomatic and supportive treatment, as no specific antidote is known or listed in the official prescribing information.

The essential mandate regarding when to seek help relates to accidental exposure by the user. Due to the active substance's antiprogestogen properties, accidental self-injection, ingestion, or spillage onto the skin constitutes a severe hazard, particularly for pregnant women and those whose pregnancy status is unknown. Under these circumstances, regulatory agencies mandate that the user must seek medical advice immediately and show the product leaflet or label to the physician. This action is required following any accidental human contact with the solution, distinguishing the regulatory concern from the observed non-systemic effects in the target animal.

Therapeutic Uses of Alizin

What Alizin Treats: Main Uses and Benefits

Alizin is a specialized veterinary medicine that supports medical management in clinical conditions where heightened physiological activity related to the reproductive cycle needs to be addressed, primarily in dogs (bitches) and cats (queens). The medicine is commonly used across domains where additional symptomatic support for specific reproductive or uterine disorders is needed.

The primary indications are the management of unwanted pregnancy and gestation, the supportive treatment for the pyometra complex, and intervention for progesterone-driven tissue growths (such as Feline Mammary Fibroadenomatosis).

This medication is applied in scenarios where short-term symptomatic assistance is needed to address established physiological states. The key therapeutic benefit is providing targeted, non-surgical intervention for these conditions. This approach may assist with maintaining the animal's sense of stability and contributes to easing the overall systemic burden by providing an alternative to surgical management in contexts where fertility preservation is a goal.

Quick Fact: Relief for Reproductive Symptoms
Common Use Contexts Post-unwanted mating; Pyometra medical management; Planned delivery facilitation.
Symptom Domains Addressed Hormonal maintenance of unwanted gestation; Uterine accumulation of purulent material; Progesterone-driven tissue proliferation.
Key Patient Benefit Provides a non-surgical option for addressing reproductive states and assists with managing life-threatening uterine pathology.

Regulatory References

  1. Summary of Product Characteristics provided by the UK Veterinary Medicines Directorate

Eligibility and Restrictions for Use

The eligibility for using Alizin (Aglepristone) is strictly defined by regulatory documents, which establish precise patient health conditions and reproductive states where the medicine is either permitted, conditional, or absolutely prohibited.

Populations for Whom Use is Contraindicated

The medicine is strictly contraindicated and must not be administered in animals presenting with the following conditions:

  • Impaired organ function: Dogs with diagnosed impaired hepatic (liver) or renal (kidney) function.
  • Endocrine and metabolic diseases: Diabetic animals or dogs with either manifest or latent hypoadrenocorticism (Addison's disease) or a genetic predisposition to it.
  • General health and hypersensitivity: Animals in poor health or those with a known hypersensitivity to the active substance, Aglepristone, or any product excipient.

Conditional and Restricted Use

Use in pregnant bitches is prohibited unless the specific purpose is the induction of abortion. Administration for this purpose is further prohibited after the 45th day post mating. In the absence of available data, the product should be used with caution in dogs with chronic obstructive-airway disease or cardiovascular disease, such as bacterial endocarditis. The official labeling lists no specific contraindications for use during lactation.

What should I know about interactions with other medicines?

Interactions with other medicines and products

This section outlines the documented interactions of Alizin (aglepristone) with other medicinal products as detailed in official regulatory sources.

Documented Interaction Categories and Implications

Interaction Domain Mechanism and Regulatory Implication
Glucocorticoids (e.g., Corticosteroids) Aglepristone is an anti-glucocorticoid and may reduce the therapeutic effect of co-administered glucocorticoid treatments.
Antifungal Agents (Ketoconazole, Itraconazole) A risk of drug interaction may exist due to a lack of complete data. Use of these agents requires caution until further information is available.
Macrolide Antibiotics (Erythromycin) A risk of drug interaction is noted in official documentation due to incomplete data. Caution is advised during co-administration.

The primary interaction constraint is based on the compound's anti-glucocorticoid activity, which necessitates monitoring to ensure that the effect of co-administered glucocorticoids is not compromised. Furthermore, official regulatory documents explicitly state that interactions with Ketoconazole, Itraconazole, and Erythromycin have not been fully studied. Due to this absence of complete information, the use of Alizin alongside these specific antifungal and antibiotic medications requires the implementation of cautionary measures as per the regulatory instruction. It is officially noted that possible interactions with other medicaments have not been studied.

Mechanism of Action

How Alizin Works

The action of Alizin (aglepristone) is centered on a targeted intervention within the reproductive hormonal signaling pathway. It is not a broad-spectrum hormonal agent but a highly specific modulator designed to interrupt the core mechanism maintaining gestation.

1. Blocking the Progesterone Signal

Alizin operates as a progesterone receptor antagonist with high binding affinity. It achieves its primary effect by binding to the progesterone receptors ( PR) found in the uterine wall and other target tissues with an affinity much greater than endogenous progesterone. This receptor-blocking action prevents the native hormone from activating the necessary cellular processes, thereby preventing the activation of the pro-gestational signal.

2. Initiating Pathway Cascades

By blocking the PR, the drug initiates a cascade that fundamentally alters the uterine environment. This shift leads to the downregulation of genes responsible for maintaining uterine quiescence and supports the release of mediators like prostaglandins. The resulting physiological effect is the loss of factors promoting uterine quiescence and the shift toward increased myometrial contractility. This targeted pathway adjustment influences core mechanisms within the reproductive signaling axis.

Dosage and Administration Information

How Alizin Is Used: Administration and Dosing

The use of Alizin (Aglepristone) is defined by a standardized protocol concerning its route of delivery, fixed dosage, and timing. The medication is supplied as a 30 mg/mL sterile solution for injection.


Administration Protocol

The sole approved route for administering Alizin is via subcutaneous injection into the tissue just beneath the skin. The formulation, which utilizes an oily vehicle, is designed exclusively for this route to ensure appropriate, sustained absorption.


Official Dosing and Schedule

Instruction Entity Official Administration Guideline
Dose Rate Fixed dose of 10 mg of Aglepristone per kg of body weight (0.33 mL of solution per kg).
Schedule Two administrations are required, given precisely 24 hours apart.
Course Duration A short, defined two-dose course is standard; a potential repeat two-dose course may be considered 10 days after the initial treatment following follow-up.

Special Procedural Constraints

The administration process includes specific technical limitations defined in the official product information. To minimize potential reactions at the injection site, the volume of solution delivered must not exceed 5 mL per single injection site. For larger animals requiring more than 5 mL, the total calculated dose must be divided and delivered into separate subcutaneous points. The injection site should be lightly massaged immediately following the delivery of the dose.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Alizin (Aglepristone)


Evidence for Pregnancy Termination in Bitches

The research for Aglepristone (Alizin) consists primarily of non-randomized field trials that included diverse populations of bitches. These studies were designed to explore the pattern of treatment completion in bitches, especially when administered within the approved window, from very early to mid-gestation (up to 45 days post-mating). Researchers monitored the process of fetal expulsion or resorption and tracked the time it took for the procedure to conclude.

The research findings describe patterns of procedural completion observed during the studies. Outcomes related to future reproductive potential were also monitored, with data indicating that many of the treated bitches were later documented as having conceived in subsequent reproductive cycles. Available data indicated that measurements of procedural completion decreased when the medicine was studied closer to the 45-day post-mating mark.

What remains uncertain is the long-term effect of receiving this treatment over multiple, consecutive reproductive cycles, as these outcomes are not well-characterized in the existing literature. Furthermore, the overall evidence base largely consists of non-randomized field trials, and comparative evidence that directly explores the differences between Aglepristone and other potential interventions is lacking.


Studies on Pyometra in Bitches and Queens

Aglepristone was studied for the medical management of pyometra (a uterine condition involving infection) in a variety of study types, including prospective, non-randomized clinical trials and numerous case reports. The research examined outcomes related to change in clinical signs and the clearance of fluid and infectious material from the uterus, typically measured through imaging. The study populations included animals often selected based on high anesthetic risk or breeding value, which characterized the context of the clinical research.

Findings describe patterns where the administration of Aglepristone, typically combined with antimicrobial therapy, was associated with measurements of change in clinical signs and uterine fluid reduction. A key limitation is that protocols for pyometra management almost always include concurrent administration of antibiotics, meaning the independent role of Aglepristone in the overall outcome is difficult to fully isolate and characterize. The sample sizes were modest in many of the published trials, contributing to lower certainty in the findings.

Key Studies & References

  1. Summary of Product Characteristics (SPC) for Alizin 30 mg/ml solution for injection for dogs and cats
  2. Summary of Product Characteristics (SPC) for Alizin: Summary of Clinical Evaluation

Frequently Asked Questions (FAQ)

Common questions about Alizin (FAQ)

Q: Is Alizin considered a contraceptive or a treatment after mating?

Official regulatory documents clarify that Alizin is described as a treatment to be used following mating. It is specifically stated in the product information that the medicine is not classified as a contraceptive.

Q: Is it possible to see behavioral changes like excitement or restlessness as a side effect?

Field trials summarized in official documentation have documented that temporary changes in behavior may occur. This includes observations of excitement, restlessness, or, conversely, depression following the administration of the medicine.

Q: What are the reported success rates for Alizin in different stages of pregnancy?

Studies summarized in regulatory sources indicate a high procedural completion rate, with the outcome being influenced by the timing of use. The reported effectiveness was approximately 99% when administered very early, and approximately 95% when administered slightly later in the approved window (21 to 45 days post-mating).

Q: Does Alizin have any long-term effects on a dog's ability to have puppies in the future?

Data suggests the medicine does not affect future reproductive ability, and treated animals have frequently been documented conceiving successfully in subsequent heat cycles. However, official information also notes that the possible long-term effects of using the treatment over multiple, consecutive reproductive cycles have not been fully characterized in the available literature.

Q: What is the chance that the treatment might fail to completely terminate the pregnancy?

Official pharmacovigilance reports indicate that a lack of complete effectiveness is rarely reported, occurring in less than 0.1% of cases. Additionally, some field trials have documented cases of partial termination.

Q: Is Alizin used for any other purpose besides pregnancy termination in registered documents?

The medicine is officially authorized and indicated only for the induction of abortion (pregnancy termination) up to 45 days after mating.

Q: Why is the timing between the two injections emphasized as critical?

The precise 24-hour interval between the two administrations is detailed in the official protocol. This specific schedule is part of the established protocol designed to achieve an effective concentration of the active substance in the body for the intended therapeutic effect.

Q: Are there research papers available that discuss the use of Alizin in cats?

The medicine is authorized for use in queens (cats) as a target species. Studies have been conducted and published regarding the use of the medicine for reproductive management and pyometra (a uterine condition involving infection) in this species.

Q: How long after the injection should an effect of Alizin be expected?

According to official documentation, the intended effect, which is the procedural completion through expulsion or reabsorption, is generally observed within seven days following the first administration.

Q: What is the difference in how Alizin works during early versus later stages of pregnancy?

The core action of the medicine—blocking the progesterone hormone receptor—remains pharmacologically the same regardless of the pregnancy stage. However, the observable physiological outcome may vary; reabsorption is more common in early pregnancy, while later use often results in expulsion with signs resembling normal birth.

Q: Can Alizin cause the body to reabsorb the pregnancy instead of resulting in a discharge?

Official pharmacological documentation indicates that the medicine's action can result in the procedural completion either through fetal expulsion or through reabsorption of the fetuses. Reabsorption is more commonly observed when the medicine is used in the earliest stages.

Q: How often are more serious side effects like uterine infection reported in clinical trials?

Data gathered from clinical field trials documented that uterine infections occurred in a small minority (3.4%) of the animals treated.

Q: What is considered a 'prolonged' vaginal discharge that warrants a check-up?

Official summaries describe conditions where veterinary consultation may be needed, such as if the discharge is described as purulent (pus-containing) or hemorrhagic (excessively bloody). Additionally, consultation is described as needed if any type of vaginal discharge persists for three weeks after the completion of the treatment course.

Q: Can the treatment cause the dog's mammary glands to appear swollen?

When the medicine is administered in the later stages of the approved use window, the termination process can be accompanied by physical signs similar to normal birth. This includes the possibility of mammary congestion or swelling.

Q: Is there evidence regarding the return to the next heat cycle after treatment with Alizin?

Official product information notes that an earlier return to the next heat cycle (oestrus) is commonly seen. The interval between heat cycles is often shortened by approximately one to three months following the administration of the medicine.

Q: Why is a follow-up check by a veterinary professional recommended after the treatment course?

A follow-up examination, typically involving ultrasound, is described in official guidelines. This procedure is used to confirm that the procedural completion was thorough and that no residual uterine content remains after the treatment.

Q: What is the meaning of the injection site reactions like 'oedema' and 'skin thickening'?

These terms describe common local inflammatory reactions that can occur due to the oily formulation used for the injection. Oedema refers to swelling, while skin thickening describes a temporary hardening or thickening of the tissue at the site where the medicine was administered.

Q: Is it safe to administer Alizin if the dog is still in heat (oestrus)?

Official guidance describes conditions where use should be avoided, suggesting that administration should wait until after the heat cycle (oestrus) has ended. This guidance is intended to reduce the possibility of a lack of expected efficacy and the potential need for a repeat treatment course.

Q: What are the possible risks if the product is accidentally self-injected?

Accidental self-injection carries a specific risk, especially for women who are pregnant or of child-bearing age. The active substance can cause severe reactions, including the alteration of fertility, and official guidance states that urgent medical advice is necessary immediately following exposure.

How should Alizin be stored and disposed of?

Storage Requirements and Stability

Alizin must be stored below 25 C and kept in its original outer carton to protect the solution from light. The shelf-life of the unopened product is 3 years.

Once the vial is opened, the in-use shelf-life is strictly limited to 28 days, after which any remaining product must be discarded.

Handling and Disposal

For safety, the medicine must be stored out of the sight and reach of children. A specific handling precaution requires that pregnant women or women of child-bearing age avoid contact with the solution due to the nature of the active ingredient.

Disposal of unused or expired Alizin must comply with national regulatory requirements and should not be discarded in household waste or via wastewater.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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