Loading...

Intellectia LogoIntellectia
AI Trading Bot
Features
Markets
News
Resources
Pricing
Get Started
  1. Home
  2. Stock
  3. SNGX
SNGX logo

SNGX Overview

-
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
OverviewStock Price PredictionTechnicalValuationFinancialsEarningsShould I BuyNews & Events
an image of Intellectia Logoan image of Intellectia

Most Trusted AI Platform for Winning Trades

TwitterYoutubeQuoraDiscordLinkedinTelegram

Copyright © 2026 Intellectia.AI. All Rights Reserved.

Company

  • Home
  • Contact
  • About Us
  • Press
  • Privacy
  • Terms of Service
  • Service Terms of Use

Resources

  • Blog
  • Tutorial
  • Help Center
  • Affiliate Program

Markets

  • Market Analysis
  • Crypto
  • Featured Screeners
  • AI Earnings Calendar
  • Market Movers
  • Stock Monitor
  • Economic Calendar
  • All US Stocks
  • All Cryptos

Tools

  • Dividend Calculator
  • Dividend Yield Calculator
  • Options Profit Calculator

Features

  • QuantAI Alpha Pick
  • SwingMax Portfolio
  • Swing Trading
  • AI Stock Picker
  • Whales Auto Tracker
  • Daytrading Center
  • Patterns Detection
  • AI Screener
  • Financial AI Agent
  • Backtesting Playground
  • AI Earnings Prediction
  • Stock Monitor
  • Technical Analysis

News

  • Overview
  • Top News
  • Daily Market Brief
  • Earnings Analysis
  • Newswire
  • Stock News
  • Crypto News
  • Institution News
  • Congress News
  • Monitor News

Compare

  • TradingView
  • SeekingAlpha
Intellectia

Loading chart...

High
1.150
Open
1.150
VWAP
1.14
Vol
162.41K
Mkt Cap
11.75M
Low
1.120
Amount
184.61K
EV/EBITDA(TTM)
--
Total Shares
10.31M
EV
3.92M
EV/OCF(TTM)
--
P/S(TTM)
--
Soligenix, Inc. is a late-stage biopharmaceutical company, which is focused on developing and commercializing products to treat rare diseases where there is an unmet medical need. The Company’s segments include Specialized Biotherapeutics, and Public Health Solutions. Its Specialized BioTherapeutics business segment is engaged in developing and focused on the commercialization of HyBryte (a proposed name of SGX301), a novel photodynamic therapy (PDT), utilizing topical synthetic hypericin activated with safe visible light for the treatment of cutaneous T-cell lymphoma (CTCL). Its Public Health Solutions segment includes development programs for RiVax, its ricin toxin vaccine candidate and SGX943, its therapeutic candidate for antibiotic-resistant and emerging infectious diseases and its vaccine programs targeting filoviruses (such as Marburg and Ebola) and CiVax, its vaccine candidate for the prevention of COVID-19 (caused by SARS-CoV-2).
Show More

Events Timeline

(ET)
2026-04-02
07:40:00
Soligenix HyBryte Study Shows Efficacy Over Valchlor
select
2026-03-26 (ET)
2026-03-26
07:40:00
Soligenix Receives EMA Orphan Drug Designation for SGX945
select
2026-03-19 (ET)
2026-03-19
07:40:00
Soligenix Publishes Summary of HyBryte Clinical Trials
select
2026-03-10 (ET)
2026-03-10
07:40:00
Soligenix SGX945 Granted Promising Innovative Medicine Designation in the UK
select
2026-02-26 (ET)
2026-02-26
07:50:00
Soligenix Receives Positive EMA Recommendation for Orphan Drug Designation for Behcet's Disease
select
2025-12-18 (ET)
2025-12-18
07:40:00
Soligenix Publishes Phase 2a Study Results for SGX945 in Behcet's Disease
select
2025-12-17 (ET)
2025-12-17
07:40:00
Soligenix Reports Significant Results for SGX302 in Psoriasis Trial
select
2025-11-19 (ET)
2025-11-19
07:33:12
Soligenix finishes patient enrollment for Phase 3 trial assessing HyBryte
select
2025-10-07 (ET)
2025-10-07
07:33:58
Soligenix's HyBryte Reaches Safety Milestone in Phase 3 Trial for T-Cell Lymphoma
select
2025-09-30 (ET)
2025-09-30
07:32:22
Soligenix Enhances European Medical Advisory Board for CTCL
select

News

PRnewswire
9.0
04-02PRnewswire
HyBryte™ Shows Promising Results in Treating Cutaneous T-Cell Lymphoma
  • Significant Treatment Success: In a 12-week comparative study, 60% of HyBryte™ patients achieved the defined treatment success level (≥50% improvement in mCAILS score), compared to only 20% for Valchlor®, indicating HyBryte™'s potential in treating cutaneous T-cell lymphoma.
  • Superior Safety Profile: HyBryte™ was well tolerated in all patients, while 60% of Valchlor® patients experienced treatment-related adverse events, including rashes and allergic reactions, suggesting that HyBryte™ may be a safer treatment option.
  • Sustained Efficacy: In the second open-label treatment cycle, 40% of patients receiving 12 weeks of HyBryte™ treatment demonstrated significant treatment response, with results showing a marked improvement compared to the placebo group, indicating that prolonged treatment can enhance patient outcomes.
  • Future Research Prospects: The FDA and EMA have mandated a second successful Phase 3 trial for marketing approval, and the follow-up study FLASH2 has successfully achieved its first safety review milestone, which is expected to accelerate the commercialization process for HyBryte™.
seekingalpha
9.5
03-31seekingalpha
Soligenix Reports FY EPS of -$2.14, Beats Estimates
  • Fiscal Year Performance: Soligenix reported a FY GAAP EPS of -$2.14, beating market expectations by $0.01, indicating a slight improvement in financial performance that may bolster investor confidence.
  • Historical Financial Data: Historical data shows that Soligenix's financial performance has fluctuated over the years; although the current EPS remains negative, the better-than-expected result could lay the groundwork for future profitability.
  • Market Reaction Analysis: Investors reacted positively to Soligenix's earnings report, which may drive the stock price up in the short term, reflecting market optimism regarding the company's future prospects.
  • Quant Rating Attention: Seeking Alpha's Quant Rating on Soligenix highlights market interest in its financial health, prompting investors to closely monitor upcoming financial reports and market developments.
PRnewswire
9.5
03-31PRnewswire
Soligenix Reports 2025 Financial Results and Upcoming Milestones
  • Clinical Trial Progress: Soligenix plans to conduct an interim analysis of the HyBryte™ clinical trial in Q2 2026, with top-line results expected in H2 2026, which will provide critical data to support the company's market potential in treating early-stage cutaneous T-cell lymphoma.
  • Deteriorating Financials: As of December 31, 2025, Soligenix reported a net loss of $11.1 million, or $2.14 per share, an increase from $8.3 million and $4.98 per share in the previous year, primarily due to rising R&D costs and decreased other income, indicating pressure on the company's financial management.
  • Increased R&D Spending: Research and development expenses rose to $7.5 million in 2025 from $5.2 million in 2024, reflecting heightened investment in studies for Behçet's Disease and CTCL, which may impact short-term financial performance but is essential for long-term product development.
  • Cash Flow Status: Soligenix ended 2025 with approximately $7.9 million in cash, which provides an operational runway into Q4 2026; however, the company is exploring various strategic options, including partnerships, mergers, and financing, to advance its late-stage pipeline.
Newsfilter
9.5
03-31Newsfilter
Soligenix Reports 2025 Financial Results and Upcoming Milestones
  • Clinical Trial Progress: Soligenix plans to conduct an interim analysis of the HyBryte™ clinical trial in Q2 2026, with top-line results expected in H2 2026, which will provide critical data for the treatment of early-stage cutaneous T-cell lymphoma, thereby enhancing the company's competitive position in the rare disease market.
  • Financial Status: As of December 31, 2025, Soligenix reported a cash balance of approximately $7.9 million; despite having no revenue, the company has sufficient funds to support operations into Q4 2026, reflecting its disciplined capital management strategy.
  • Increased R&D Investment: Research and development expenses rose to $7.5 million in 2025 from $5.2 million in 2024, primarily driven by costs associated with the Phase 2 study for Behçet's Disease and the ongoing confirmatory Phase 3 study for CTCL, indicating the company's commitment to investing in rare disease treatments.
  • Regulatory Progress: The company received orphan drug designation for dusquetide from the European Commission in March 2026, which not only enhances the market potential for SGX945 but may also pave the way for future financing and partnership opportunities.
PRnewswire
8.5
03-26PRnewswire
Soligenix Receives EU Orphan Drug Designation for SGX945
  • Orphan Drug Designation: Soligenix's SGX945 has received orphan drug designation from the European Commission for treating Behçet's Disease, based on positive evaluations of its clinical trial results by the EMA, marking a significant advancement in addressing unmet medical needs.
  • Market Exclusivity: Following the orphan drug designation, SGX945 will enjoy a 10-year period of market exclusivity in the EU, which will enhance the company's competitive edge and attract more investor interest in its product development.
  • Clinical Trial Results: In a Phase 2a clinical trial involving 8 patients with Behçet's Disease, SGX945 demonstrated a 40% improvement in efficacy compared to a 37% improvement in the placebo group, indicating its potential in treating difficult-to-manage oral ulcers.
  • Intellectual Property Protection: Soligenix holds a strong intellectual property position in its IDR technology platform, including patents for the composition of dusquetide and related analogs, which will further strengthen its market position in the biopharmaceutical sector.
Newsfilter
8.5
03-26Newsfilter
Soligenix Receives EU Orphan Drug Designation for SGX945
  • Orphan Drug Designation: Soligenix's SGX945 has received orphan drug designation from the European Commission for treating Behçet's Disease, marking a significant advancement in addressing unmet medical needs and is expected to enhance the company's market competitiveness.
  • Clinical Trial Results: In the Phase 2a clinical trial, SGX945 demonstrated biological efficacy and safety, with the treatment group showing a 40% improvement in oral ulcers compared to the placebo group, laying a solid foundation for future market approval.
  • Market Potential: With approximately 1 million people affected by Behçet's Disease globally, the successful development of SGX945 could provide new treatment options for these patients, potentially significantly increasing the company's revenue prospects.
  • Intellectual Property Advantage: Soligenix holds a strong intellectual property position in its IDR technology platform, and the orphan drug and fast track designations for SGX945 will provide legal protection and market exclusivity for its future commercialization efforts.
Wall Street analysts forecast SNGX stock price to rise
1 Analyst Rating
Wall Street analysts forecast SNGX stock price to rise
1 Buy
0 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
10.00
Averages
10.00
High
10.00
Current: 0.000
sliders
Low
10.00
Averages
10.00
High
10.00
Alliance Global Partners
James Molloy
Buy
downgrade
$10 -> $6
AI Analysis
2025-07-16
Reason
Alliance Global Partners
James Molloy
Price Target
$10 -> $6
AI Analysis
2025-07-16
downgrade
Buy
Reason
Alliance Global Partners analyst James Molloy lowered the firm's price target on Soligenix to $6 from $10 and keeps a Buy rating on the shares after the company reported recent corporate updates and clinical progress of HyBryte. The firm says its price target represents a sum-of-the-parts.

Valuation Metrics

The current forward P/E ratio for Soligenix Inc (SNGX.O) is 12.32, compared to its 5-year average forward P/E of -0.86. For a more detailed relative valuation and DCF analysis to assess Soligenix Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-0.86
Current PE
12.32
Overvalued PE
2.67
Undervalued PE
-4.38

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-0.00
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
0.00
Undervalued EV/EBITDA
-0.00

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PS
17.29
Current PS
0.00
Overvalued PS
28.86
Undervalued PS
5.73

Financials

AI Analysis
Annual
Quarterly

Related Community Screener

low float high volume medical stock
Intellectia · 22 candidates
Sector: Healthcare, Healthcare Services & Equipment, Pharmaceuticals & Medical ResearchVolume: >= 1,000,000List Exchange: XNYS, XNAS, XASEFloating Shares: <= 30,000,000
Ticker
Name
Market Cap$
top bottom
AKAN logo
AKAN
Akanda Corp
1.66M
IBIO logo
IBIO
iBio Inc
60.11M
BIAF logo
BIAF
bioAffinity Technologies Inc
21.32M
AZTR logo
AZTR
Azitra Inc
3.82M
KPTI logo
KPTI
Karyopharm Therapeutics Inc
109.27M
SNGX logo
SNGX
Soligenix Inc
12.20M

Whales Holding SNGX

Trading Trends

    Insider
    Hedge Fund
    Congress Trading

People Also Watch

Frequently Asked Questions

What is Soligenix Inc (SNGX) stock price today?

The current price of SNGX is 1.14 USD — it has decreased -0.87

What is Soligenix Inc (SNGX)'s business?

Soligenix, Inc. is a late-stage biopharmaceutical company, which is focused on developing and commercializing products to treat rare diseases where there is an unmet medical need. The Company’s segments include Specialized Biotherapeutics, and Public Health Solutions. Its Specialized BioTherapeutics business segment is engaged in developing and focused on the commercialization of HyBryte (a proposed name of SGX301), a novel photodynamic therapy (PDT), utilizing topical synthetic hypericin activated with safe visible light for the treatment of cutaneous T-cell lymphoma (CTCL). Its Public Health Solutions segment includes development programs for RiVax, its ricin toxin vaccine candidate and SGX943, its therapeutic candidate for antibiotic-resistant and emerging infectious diseases and its vaccine programs targeting filoviruses (such as Marburg and Ebola) and CiVax, its vaccine candidate for the prevention of COVID-19 (caused by SARS-CoV-2).

What is the price predicton of SNGX Stock?

Wall Street analysts forecast SNGX stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for SNGX is10.00 USD with a low forecast of 10.00 USD and a high forecast of 10.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Soligenix Inc (SNGX)'s revenue for the last quarter?

Soligenix Inc revenue for the last quarter amounts to 0.00 USD, decreased

What is Soligenix Inc (SNGX)'s earnings per share (EPS) for the last quarter?

Soligenix Inc. EPS for the last quarter amounts to -0.29 USD, decreased -75.63

How many employees does Soligenix Inc (SNGX). have?

Soligenix Inc (SNGX) has 13 emplpoyees as of April 10 2026.

What is Soligenix Inc (SNGX) market cap?

Today SNGX has the market capitalization of 11.75M USD.