Landmark 308 · Trial in people

AKST4290 (TEAL)

Did not beat placebo in 110 people over 12 weeks. Both groups improved a little, and placebo slightly more.

In short

A 110-person, 12-week Phase 2 trial of a pill that blocks the immune receptor CCR3 found no advantage over placebo on its main motor measure.

What it is
Trial in people
Outcome
Did not work
When
2020–2021
Size
110 people · Phase 2
Approach
Look beyond the brain
Research lane
Inflammation & immunity
Trial registry
NCT04369430
Last checked
19 Oct 2026

The research record

This is the project's file for this landmark, as written and checked. Sources are listed at the end; anything not yet confirmed is marked "Not yet verified".

Who

Alkahest, Inc. Sites included the US, Estonia and Germany. Alkahest had licensed the molecule from Boehringer Ingelheim (per a search summary of the conference abstract; not checked at source).

What happened

CCR3 is a receptor on immune cells that responds to eotaxin (CCL11), a signal that rises with age. AKST4290 blocks it. The idea is that this calms brain inflammation, following landmark 52, which found activated immune cells in the nigra.

TEAL (NCT04369430) enrolled people with Parkinson's on stable dopamine treatment (Hoehn and Yahr stage 2.5 or less). Of 110 randomised, 55 got 400 mg AKST4290 twice a day and 55 placebo, for 12 weeks. About 93 finished (46 and 47). The main measure was the change in off-medication movement score (MDS-UPDRS Part 3; lower is better). The drug group changed by minus 4.2 points and the placebo group by minus 5.1, so placebo improved slightly more. Both groups improved, which is common in short trials with a placebo. Serious adverse events: 1 of 52 on the drug and 3 of 55 on placebo.

Some secondary scores favoured the drug (for example the patient quality-of-life mobility score and the clinician severity score), but the primary result was null.

Why it moved us toward a cure

This was the first controlled test of a drug aimed at the immune system's chemokine signals in Parkinson's. A null result over 12 weeks does not rule out slower effects, but the measure was a symptom score, not progression, so the trial could not show slowing even if the drug worked.

Outcome

Dead end for this drug in this design. I found no Phase 3 plan. Alzforum (updated Oct 2021) says no results were made public.

Sources

How it connects

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