Nefiracetam

guinea pig

Also seen as: DM-9384, DM9384

The Dose Guy’s verdict
Sep 1, 2026
5 sources

Nefiracetam has an interesting mechanism and real human trials, which puts it ahead of most racetams on paper. The problem is testicular toxicity in dogs at high doses, with sperm motility and morphology both hit. The human trials tested post-stroke depression and apathy and came back weak and mixed. If you want a racetam, aniracetam and piracetam are cleaner picks with longer track records. If you want this one specifically, read the dog data first.

Would I take it?Not with that toxicity flag in the room.

What it is

Nefiracetam is a fat-soluble pyrrolidone nootropic, part of the racetam family but with a wider mechanism than most of its siblings. Where piracetam and aniracetam work primarily through AMPA modulation, nefiracetam also potentiates NMDA currents, the glutamate receptor type tied to learning and plasticity, through a protein kinase C pathway and enhances nicotinic acetylcholine receptor signaling, the system that supports attention and memory encoding. That triple-channel profile across glutamate and cholinergic systems is what drew clinical interest.

That mechanistic breadth is what drew clinical interest for mood and cognition after stroke, where multiple neurotransmitter systems are disrupted at once. It also means the compound touches more biology than a simple racetam, which cuts both ways when the safety data has gaps.

What the research shows

The human trials exist but underwhelm. The animal safety signal is the finding that follows you home:

In 159 post-stroke depression patients, nefiracetam did not reach significance over placebo. Response rates exceeded 70% in both groups, leaving little room for a drug effect.J Neuropsychiatry 2008 · RCT · n=159
Among 70 stroke patients with depression and apathy, 900 mg daily produced a greater Apathy Scale change than 600 mg daily or placebo after at least four weeks. The one positive signal in the clinical program.J Neuropsychiatry 2009 · phase 2 · n=70
In 13 post-stroke apathy patients, 900 mg daily for 12 weeks did not produce a significant between-group difference from placebo.J Stroke Cerebrovasc Dis 2016 · RCT · n=13
In rat cortical neurons, 10 nM nefiracetam increased NMDA current to 170% of control through interaction with the glycine binding site.J Pharmacol Exp Ther 2003 · rat neurons
Male beagle dogs given 180 or 300 mg/kg daily for four weeks developed moderate or severe seminiferous atrophy, decreased sperm motility, and increased malformed sperm.Reprod Toxicol 2004 · dogs
No trial has tested nefiracetam for cognitive enhancement in healthy people. The entire clinical database is post-stroke.as of Aug 2026

Realistic protocols

If you run nefiracetam despite the toxicity flag, most people settle at 600 to 900 mg daily, split into two or three doses. The clinical trials used 600 to 900 mg daily in post-stroke patients. The racetam community generally pairs it with a choline source like alpha-GPC to support the acetylcholine demand, the same pairing used across the racetam family. Fat-soluble, so take it with food. The compound clears quickly, which is why splitting doses matters for steady levels.

The toxicity question: the dog seminiferous atrophy appeared at 180 mg/kg and above. A 70 kg person taking 800 mg daily sits at roughly 11 mg/kg, well below that line. But the margin is not so wide that you ignore it, especially with no long-term human reproductive safety data. If you are a man concerned about fertility, skip this racetam.

Start200 mg 2x/dayWith food and a choline source. Low start to assess tolerance.
Standard300 mg 2–3x/dayThe range most users settle at. Split doses keep levels steadier.
Ceiling900 mg/dayThe trial max. No reason to push past it.

Side effects

The racetam side profile is generally mild, but nefiracetam carries a flag the others do not:

commonHeadache, the classic racetam complaint, usually manageable with adequate choline intake.
monitorTesticular toxicity in dogs at 180+ mg/kg daily. Human reproductive safety at chronic doses has not been studied. Men should weigh this before committing to a run.
anecdotalDrowsiness or mild sedation at higher doses, sometimes reported alongside improved mood. Distinct from the stimulating feel of some racetams.
monitorCYP3A4 principally mediates formation of one key metabolite, so strong 3A4 inhibitors like ketoconazole or clarithromycin could raise levels.

Where to buy

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