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CLAIM #2724 · AbbVie Inc (ABBV) · 2025Q4 earnings call · Feb 4, 2026 · due Dec 31, 2026

Approval decisions in Europe and Japan are expected later this year.

Roopal Thakkar · Chief Scientific Officer

PENDING
graded after results covering Dec 31, 2026 are reported

How to check this claim

Look at: Regulatory approval decision status for Qlipta (atogepant) in Europe (EMA) and Japan (PMDA)

It came true if: At least one formal approval decision (approval or rejection) issued by either EMA or Japan's PMDA for Qlipta on or before 2026-12-31

Where: Company press releases / regulatory agency decision databases (EMA CHMP opinions, PMDA approvals) and AbbVie quarterly earnings commentary

In context

ill experiencing motor fluctuations. This year, a phase two study assessing gemmibot A in essential tremor will begin. Essential tremor is the most common movement disorder and an area with considerable need for effective and tolerable therapies. Unlike most patients with spasticity, patients with essential tremor typically have normal strength. Therefore, it is important that neighboring muscles are not inadvertently affected, and this is by toxin diffusion. Our new toxin is highly potent and has the potential for less spread to neighboring muscles, making it well-suited for treating essential tremor. In migraine, the phase three ECLIPSE trial evaluating QLIPTA for acute treatment of migraine met its primary and key secondary endpoints, with Qlipta demonstrating superiority over placebo. Approval decisions in Europe and Japan are expected later this year. Our phase three studies evaluating Qlipta and UBRELVY for menstrual migraine prevention are progressing well, with data from both trials expected in the second half of this year. Regulatory submission for Qlipta in Europe is anticipated later this year, and for UBRELVY in the US in 2027. Menstrual migraine is a distinct subtype affecting nearly 15% of women with migraine. Attacks are considered more difficult to treat, more disabling, last longer, and have a higher tendency to recur. There is a clear need for more effective treatment for this form of migraine. In the area of psychiatry, several readouts and study starts are planned this year across multiple programs. Our dose escalation study continues for ameraclidine in schizophrenia, with the 75-milligram dose cleared and 100 milligram

Verify independently

SEC filings for ABBV · Claim quote is verbatim from the 2025Q4 earnings call.