Capricor Therapeutics Deramiocel FDA Approval Decision

FDA Approval·
·
Added

About This Event

The FDA's PDUFA target action date arrives for Capricor Therapeutics' Deramiocel Biologics License Application for Duchenne muscular dystrophy cardiomyopathy.

Why This Event Matters

Regulatory milestones can be important for biotech and pharmaceutical names because decisions may affect timelines, labeling, and commercial prospects. Outcomes are uncertain until confirmed by the company or agency materials; this listing is informational. The date shown is August 21, 2026 (America/New_York).

Source summary: The FDA's PDUFA target action date arrives for Capricor Therapeutics' Deramiocel Biologics License Application for Duchenne muscular dystrophy cardiomyopathy.

This listing is associated with CAPR. Market participants may watch these names around the event window for volatility or news flow.

Event Details

Occurs

Fri, Aug 21, 2026 · 10:00 AM EDTVerified

Related Tickers

Impact Likelihood

95%

Source

Created By

catacal

Frequently Asked Questions

What is Capricor Therapeutics Deramiocel FDA Approval Decision?
It is a stock market catalyst entry on Catacal—an event or release investors and traders may monitor. Details are summarized from the cited source and may be updated over time.
When is Capricor Therapeutics Deramiocel FDA Approval Decision?
The calendar shows Aug 21, 2026 (America/New_York). Verify the exact time and any changes using the source link when planning around the event.
Why does Capricor Therapeutics Deramiocel FDA Approval Decision matter for investors?
Regulatory outcomes can change timelines and risk profiles for drug and device developers.
Which stocks or sectors could be affected?
Symbols linked to this listing include CAPR; other names in the same industry group may also move with related news.
How is this event categorized?
Catacal groups this entry under "FDA Approval" for navigation. Categories help you find comparable catalysts and build a week-by-week watchlist.

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