Independent Market Access and Reimbursement Risk Assessment.

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Ryeqo for treating symptoms of endometriosis

As of April 2025, MARA’s assessment finds Ryeqo’s reimbursement risk concentrated in comparator selection, with cost effectiveness a strength; the current MARA Rating and full rationale are available in the report.

The assessment also weighs clinical effectiveness: how much additional benefit the drug demonstrated over the care patients already receive — the first question every payer asks. The strength recorded in cost effectiveness carries weight because that domain asks whether the price asked stands in a defensible relationship to the benefit delivered — the core of most European reimbursement decisions.

Gynecology

What payers will ask

Is the clinical benefit the kind payers reward? — Clinical effectiveness

Relugolix CT shows moderate benefit over current care, with clinical trial evidence indicating a significant reduction in dysmenorrhoea and non-menstrual pelvic pain compared to placebo. However, the lack of direct comparisons with standard treatments like GnRH agonists and surgery limits the strength of the evidence.

Does the economic case hold at the expected price? — Cost effectiveness

The cost-effectiveness estimates for relugolix CT are within the acceptable range for Healthcare resources, suggesting it is a cost-effective option compared to existing treatments. The committee concluded that the ICERs are acceptable, supporting its economic viability.

Is there quality-of-life evidence payers weigh? — Quality of life

The evidence suggests that relugolix CT improves quality of life for patients with endometriosis, as indicated by the significant reduction in pain levels. However, the data on HRQoL improvements are not extensively detailed, leading to a moderate rating.

Does the safety profile hold up for payers? — Safety and Adverse Effects

Relugolix CT has a very good safety profile with mostly mild to moderate adverse events reported. The evidence indicates that serious adverse events are rare, supporting a strong tolerability rating.

Was the drug compared against what payers expect? — Comparator Selection

While GnRH agonists are identified as relevant comparators, the absence of direct head-to-head trials with these treatments raises concerns about the robustness of the evidence. The committee noted that surgery could also be a relevant comparator, which was not included in the initial analysis.

Is the population defined the way payers need it? — Patient Population and Subgroups

The trial population is broadly representative of the intended patient population, with a focus on adults of reproductive age who have had prior treatments for endometriosis. However, there are some limitations in subgroup analyses.

Does the drug fit how care is delivered and paid for? — Care Pathway Integration

Relugolix CT can be integrated into existing care pathways with minor adjustments, as it offers an oral administration route that is more convenient than injectable options. This enhances its feasibility in clinical practice.

Are the wider system costs understood? — Resource Use and Cost Implications

The resource implications of relugolix CT are manageable, with the potential for cost savings due to its oral administration and reduced need for hospital visits compared to injectable treatments.

Would the evidence survive payer scrutiny? — Evidence Quality and Robustness

The evidence base is supported by two phase 3 RCTs, which provide strong data. However, the reliance on indirect comparisons and some methodological concerns limit the overall robustness.

How exposed is the case to uncertainty? — Uncertainty, Sensitivity, and Broader Impacts

While there are uncertainties regarding the long-term effects and utility values used in the economic model, the overall context supports the use of relugolix CT, particularly given the unmet need in endometriosis treatment.

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