Crinetics Pharmaceuticals Aktie

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WKN DE: A2JQTJ / ISIN: US22663K1079

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23.09.2025 10:45:43

CRNX FDA Catalyst Alert: Could Paltusotine Decision Reshape Endocrine Drug Market?

(RTTNews) - Crinetics Pharmaceuticals Inc. (CRNX) is approaching a watershed moment in its corporate and clinical trajectory. On September 25, 2025, the FDA is expected to announce its decision on the company's New Drug Application or NDA for paltusotine, a once-daily oral somatostatin receptor type 2/SST2 agonist developed for the treatment and long-term maintenance of acromegaly in adults.

If approved, paltusotine would become the first and only nonpeptide SST2 agonist available in oral form, offering a transformative alternative to the current standard of care, monthly injectable peptide analogs that are often painful, cumbersome, and logistically challenging for patients.

The drug's clinical potential is backed by robust Phase 3 data from the PATHFNDR-1 and PATHFNDR-2 trials, which demonstrated sustained IGF-1 control and symptom relief in both previously treated and medically untreated patients.

This FDA decision is more than a regulatory milestone; it's a make-or-break inflection point for Crinetics. A green light would confirm years of work on paltusotine and open the door to a new treatment option for acromegaly, a condition that hasn't seen much change in how it's managed. The company has already started preparing for a possible launch, building its sales and medical teams and working with payers and doctors who treat endocrine disorders.

Conversely, a rejection or delay could reverberate across Crinetics' pipeline and weigh on market sentiment. With paltusotine as its lead candidate, the company's valuation and strategic momentum hinge heavily on FDA approval. While the agency has indicated that an advisory committee meeting is not anticipated, the absence of such a forum does not guarantee a smooth path forward.

With $1.2 billion in cash and equivalents as of June 30, 2025, the company has runway into 2029, positioning it to execute across multiple programs regardless of the FDA's decision.

All eyes now turn to the FDA, where the outcome carries weight well beyond a single approval. The stakes couldn't be higher. Click here to read more on CRNX.

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