I'm SHORT $MNOV. They changed the test mid-trial to make life...

They changed the test mid-trial to make life easier.
They can't change the drug.
It fails🧵
To get in, patients used to need at least 8% liver fat on MRI. Now any fatty liver at all on FibroScan will do.
Head to head against liver biopsies, the MRI was far more accurate than FibroScan.
A blurrier ruler hides small changes. And patients with less fat have less fat to lose.
Easier to sign people up. Harder to win.
A year later the MRI words quietly vanished, with nothing in their place.
FibroScan's first appearance in an SEC filing: one slide, two years after the switch.
Investors paid for this trial. They found out last.
The only human data for this drug in this disease is a tiny pilot. No placebo group. Everyone got the drug. 19 patients, when their own 2016 slides planned 40.
They stopped it early for "significant positive results." Then the actual results took nearly five years to show up publicly.
When they finally did, the main goal was flat and liver fat hadn't moved.
In 2022 mnov announced that "in the next study" they'd check liver fat by MRI. Like it was a fresh idea.
Then, seven months into that study, they switched to the blurrier scan anyway.
Result: basically zero.
Search every MNOV SEC filing for "cholesterol efflux." One hit: the 2016 slide promising it. The result never made it into a single filing.
Last November they bragged about cholesterol efflux in immune cells. In cells, a miracle. In humans, a zero.
July 2020, more than two years after primary completion, CMO Kazuko Matsuda signed SAP v2.0. It moved the triglyceride primary to week 8.
The protocol promised the SAP "prior to database lock." The registry said 12 weeks right up until results posted.
Changing the rules one day early got $CAPR torched. Medicinova went two years late.
Start from someone's worst reading and the number tends to fall on its own, drug or no drug. It's like taking your "before" photo right after Thanksgiving dinner.
The new trial has a placebo group. That free drop goes to both groups now.
Medicinova says it blocks one of the same enzymes as cilostazol, an old generic pill. Cilostazol's FDA label: triglycerides down 15% versus placebo.
It also carries the FDA's scariest warning: don't give it to heart failure patients.
Best case, they spent ten years reinventing a generic with a black box.
In 2016 the FDA said lowering triglycerides in people on statins doesn't prove a drug prevents heart attacks or strokes. It stripped two drugs of part of their approval over it.
The first study the FDA cited was in type 2 diabetics. The same kind of patients as this trial.
MNOV's own CMO co-authored an earlier open-label study of this drug in ALS at up to 100 mg a day.
31% of patients quit over drug-related side effects. No significant reduction in PET signal or neurofilament.
COMBAT-ALS runs the same top dose.
David Crean, this month, on the small ALS study that launched the big trial: "It was small. The treatment groups were imbalanced." The results were "not truly definitive evidence of efficacy."
Then he brought up Relyvrio, the ALS drug pulled after its big trial flopped. Bold move for a sales pitch.
Dec 29, 2025: MNOV hires Lucid Capital Markets to sell up to $50 million of new stock, for a 3% cut.
Jan 5, 2026: Lucid starts publishing research on the stock.
Aug 19, 2026, six weeks before results: new contracts for CEO Yuichi Iwaki and Matsuda. If Iwaki is pushed out around a sale, he walks with two years of pay plus two years of bonus.
Everybody gets paid. Except you.
When a company tells you a result doesn't matter right before it lands, it's not because they're optimistic.
Headline: "MediciNova Announces Positive Clinical Results."
Third paragraph: the drug missed the main goal the trial was designed to hit.
Their 2007 deck promised the next big MS trial "as early as 08Q2." Kids born that quarter can vote now. Still no big MS trial.
This trial misses. Short it.
And if the headline says "positive" anyway, short more. Yuichi Iwaki has done it before.
$MNOV goes to $1-1.5.





















