Key Performance
More- Earnings Score: N/A
- Momentum Score: 77
- True Yield: N/A
- Financial Health Score: N/A
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Latest Research & News
U.S. stock futures rose on Tuesday following Memorial Day, with the S&P 500 and Nasdaq 100 gaining 0.52% and 0.73% respectively. Despite U.S. defensive strikes on Iranian missile sites, markets remained resilient as oil prices fell and Iran negotiations progressed. Key movers included Elbit Systems jumping 8.26% on a $1.4B military contract, Intuitive Machines soaring 10.27% on a NASA lunar contract, and SCYNEXIS plunging 16.38% after announcing a reverse stock split.
05/26/2026, 8:47 AM • Benzinga
U.S. stock futures rose on Tuesday following Memorial Day, with the S&P 500 and Nasdaq 100 gaining 0.52% and 0.73% respectively. Despite U.S. defensive strikes on Iranian missile sites, markets remained resilient as oil prices fell and Iran negotiations progressed. Key movers included Elbit Systems jumping 8.26% on a $1.4B military contract, Intuitive Machines soaring 10.27% on a NASA lunar contract, and SCYNEXIS plunging 16.38% after announcing a reverse stock split.
05/26/2026, 5:44 AM • Benzinga
SCYNEXIS Announces Inducement Awards Under Nasdaq Listing Rule 5635(c)(4)
SCYNEXIS, Inc. approved inducement equity awards for a new Vice President on April 30, 2026, consisting of stock options to purchase 125,000 shares at $0.93 per share and 20,000 restricted stock units. The awards were granted under the company's 2015 Inducement Award Plan in accordance with Nasdaq regulations.
05/06/2026, 9:15 PM • GlobeNewswire
SCYNEXIS announced the completion of its acquisition of PXL-770 (now SCY-770), a novel AMPK activator for treating ADPKD, the leading genetic cause of end-stage renal failure. Under the deal, SCYNEXIS will pay $8 million upfront with up to $188 million in potential milestone payments. The company plans to initiate a Phase 2 proof-of-concept study in Q4 2026 with early efficacy readout expected in H2 2027. SCY-770 has received FDA Orphan Drug Designation.
03/31/2026, 6:40 AM • Benzinga
SCYNEXIS Completes Transfer of BREXAFEMME® New Drug Application to GSK
SCYNEXIS has transferred its BREXAFEMME New Drug Application to GSK, enabling potential regulatory interactions for relaunching the drug for vulvovaginal candidiasis. SCYNEXIS will receive potential net sales milestones and royalties from GSK.
11/19/2025, 7:00 AM • GlobeNewswire
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Company Profile
SCYNEXIS, Inc., a biotechnology company, engages in drug development for the treatment and prevention of difficult-to-treat and drug-resistant fungal infections in the United States. The company offers BREXAFEMME for the treatment of patients with vulvovaginal candidiasis and for the reduction in the incidence of recurrence. It also develops SCY-247, which is in Phase I clinical trial for the treatment of invasive fungal infections. The company was formerly known as SCYNEXIS Chemistry & Automation, Inc. and changed its name to SCYNEXIS, Inc. in June 2002. SCYNEXIS, Inc. was incorporated in 1999 and is headquartered in Jersey City, New Jersey.