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CLAIM #2723 · AbbVie Inc (ABBV) · 2025Q4 earnings call · Feb 4, 2026 · due Dec 31, 2026

This year, a phase two study assessing gemmibot A in essential tremor will begin.

Roopal Thakkar · Chief Scientific Officer

PENDING
graded after results covering Dec 31, 2026 are reported

How to check this claim

Look at: Initiation status of phase two study of gemmibot A (toxin) in essential tremor

It came true if: Study listed as initiated/recruiting (or further along) on a clinical trial registry, or company states study has begun, on or before 2026-12-31

Where: Clinicaltrials.gov registry entry or company pipeline update / press release / earnings call commentary

In context

le myeloma, with an objective response rate readout anticipated in the second half of this year. A phase two study of ententamig plus daratumumab in frontline transplant-ineligible patients was recently initiated. Additionally, a phase three study in second-line evaluating entantamig with pomalidomide is expected to begin by early 2027. Turning to neuroscience, in our movement disorder programs, an approval decision is anticipated in the third quarter for tevapadon in Parkinson's disease. As a highly effective treatment for motor symptoms, with low rates of dyskinesia, edema, sedation, and impulse control disorder, tevapadon has the potential to be an important new treatment option, both as a monotherapy and as an adjunct to levocarbidopa in patients still 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 UBR

Verify independently

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