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SNGX Overview

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ET
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Intellectia

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High
1.280
Open
1.240
VWAP
1.26
Vol
91.99K
Mkt Cap
12.71M
Low
1.230
Amount
115.61K
EV/EBITDA(TTM)
--
Total Shares
10.09M
EV
2.18M
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)
2026-03-10
07:40:00
Soligenix SGX945 Granted Promising Innovative Medicine Designation in the UK
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2026-02-26 (ET)
2026-02-26
07:50:00
Soligenix Receives Positive EMA Recommendation for Orphan Drug Designation for Behcet's Disease
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2025-12-18 (ET)
2025-12-18
07:40:00
Soligenix Publishes Phase 2a Study Results for SGX945 in Behcet's Disease
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2025-12-17 (ET)
2025-12-17
07:40:00
Soligenix Reports Significant Results for SGX302 in Psoriasis Trial
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2025-11-19 (ET)
2025-11-19
07:33:12
Soligenix finishes patient enrollment for Phase 3 trial assessing HyBryte
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2025-10-07 (ET)
2025-10-07
07:33:58
Soligenix's HyBryte Reaches Safety Milestone in Phase 3 Trial for T-Cell Lymphoma
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2025-09-30 (ET)
2025-09-30
07:32:22
Soligenix Enhances European Medical Advisory Board for CTCL
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2025-09-04 (ET)
2025-09-04
07:33:16
Soligenix's ThermoVax Platform Demonstrates Effectiveness in Vaccine Stability
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2025-08-18 (ET)
2025-08-18
07:32:03
Soligenix's dusquetide receives Orphan Drug Designation for Behcet's Disease
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2025-08-13 (ET)
2025-08-13
17:57:28
Soligenix receives FDA orphan designation for dusquetide
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link

News

PRnewswire
8.5
03-10PRnewswire
Soligenix Receives PIM Designation for SGX945 in the UK
  • PIM Designation Achieved: Soligenix's SGX945 (dusquetide) has received Promising Innovative Medicine (PIM) designation from the UK's Medicines and Healthcare Products Regulatory Agency (MHRA), marking a significant advancement in its treatment for Behçet's Disease and potentially accelerating access through the Early Access to Medicines Scheme (EAMS).
  • Clinical Data Validation: The MHRA's recognition of dusquetide's compliance with PIM criteria is based on Phase 2 clinical trial data, indicating its potential to provide earlier treatment options for patients, thereby improving their quality of life and addressing unmet medical needs.
  • Significant Efficacy: SGX945 demonstrated a 40% improvement compared to placebo after four weeks of treatment, surpassing apremilast's 37% improvement, highlighting its competitive edge in clinical applications and likely attracting increased investor interest.
  • Strong IP Position: Soligenix holds robust intellectual property rights in its IDR technology platform, including patents for the composition of dusquetide, which provides legal protection for future market commercialization and enhances the company's competitiveness in the biopharmaceutical sector.
Newsfilter
9.0
03-10Newsfilter
Soligenix Receives UK PIM Designation for SGX945
  • PIM Designation Achieved: Soligenix's SGX945 (dusquetide) has received Promising Innovative Medicine (PIM) designation from the UK's MHRA, marking a significant advancement in treating Behçet's Disease and providing patients with earlier access to groundbreaking therapies.
  • Clinical Data Support: Based on Phase 2 clinical data, dusquetide is expected to offer significant advantages in treating Behçet's Disease, potentially improving patients' quality of life and alleviating symptoms effectively.
  • Substantial Market Potential: With over 1 million patients worldwide suffering from Behçet's Disease, the successful commercialization of SGX945 could fill a critical market gap, addressing the urgent need for effective treatments and potentially generating significant revenue.
  • Safety Validation: In a Phase 1 study involving 84 healthy volunteers, SGX945 demonstrated excellent safety and tolerability, with significantly reduced side effects compared to existing treatments, thereby enhancing its competitive position in the market.
PRnewswire
8.5
02-26PRnewswire
Soligenix Receives Positive EMA Orphan Drug Recommendation
  • Orphan Drug Qualification: Soligenix announced that its SGX945 (active ingredient dusquetide) received a positive recommendation from the EMA Committee for Orphan Medicinal Products, marking a significant advancement in treating Behçet's Disease and expected to provide a 10-year marketing exclusivity period, enhancing its competitive edge in the rare disease sector.
  • Clinical Trial Results: In the Phase 2a clinical trial, SGX945 demonstrated biological efficacy and safety in 8 patients with Behçet's Disease, showing a 40% improvement over the placebo group within 4 weeks, laying a solid foundation for future market approval.
  • Significant Market Demand: With approximately 1 million people affected by Behçet's Disease globally, particularly in Turkey and Europe, SGX945 presents substantial market potential to address unmet medical needs, potentially leading to significant revenue growth for the company.
  • Intellectual Property Advantage: Soligenix holds a strong intellectual property position in its IDR technology platform, including patents for the composition of dusquetide, which will provide crucial legal protection and competitive advantages in future product development and market commercialization.
Newsfilter
8.5
02-26Newsfilter
Soligenix Receives Positive EMA Orphan Drug Recommendation
  • Orphan Drug Qualification: Soligenix announced that its SGX945 (active ingredient dusquetide) received a positive recommendation from the EMA's Committee for Orphan Medicinal Products, marking a significant advancement in the treatment of Behçet's Disease and expected to provide a 10-year market exclusivity period.
  • Clinical Trial Results: In the Phase 2a clinical trial, SGX945 demonstrated biological efficacy and safety in 8 patients with Behçet's Disease, showing a 40% improvement compared to the placebo group after 4 weeks, laying the groundwork for future market approval.
  • Significant Market Demand: With approximately 1 million people affected by Behçet's Disease globally, particularly in Turkey and Europe, the urgent need for effective treatments highlights the potential market impact of SGX945, significantly enhancing Soligenix's position in the biopharmaceutical sector.
  • Intellectual Property Protection: Soligenix holds a strong intellectual property position in its IDR technology platform, including patents for the composition of dusquetide, which will provide crucial support for the company's future product development and market commercialization efforts.
PRnewswire
8.5
02-24PRnewswire
Soligenix to Present at BIO Investment Summit
  • Presentation Schedule: Soligenix's CEO, Dr. Christopher J. Schaber, will present at the BIO Investment & Growth Summit on March 2, 2026, at 3 PM in Miami, showcasing the company's advancements in treating rare diseases, which is expected to attract investor interest.
  • Product Development Progress: The company is advancing HyBryte™ (SGX301) as a novel photodynamic therapy, having successfully completed the second Phase 3 clinical trial, and if regulatory approvals are obtained, it will provide new treatment options globally, significantly enhancing the company's competitiveness in the biopharmaceutical sector.
  • Public Health Solutions: Soligenix's Public Health Solutions segment is developing vaccine candidates like RiVax®, supported by government grants from NIAID and BARDA, demonstrating the company's strategic positioning in addressing bioterror threats and strengthening its market presence.
  • Future Outlook and Risks: Despite achieving statistically significant results in HyBryte™ clinical trials, the company faces regulatory challenges from the FDA and EMA, and future product development and commercialization efforts may be impacted by clinical trial delays and funding shortages, necessitating careful navigation of market competition.
Newsfilter
8.5
02-24Newsfilter
Soligenix to Present at BIO Investment Summit
  • Presentation Schedule: Soligenix's CEO, Dr. Christopher J. Schaber, will present at the BIO Investment & Growth Summit on March 2, 2026, at 3 PM in Miami, showcasing the company's advancements in rare disease treatments, which is expected to attract investor interest.
  • Product Development Progress: The company is advancing its HyBryte™ (SGX301) into Phase 3 clinical trials, having successfully completed the second Phase 2 study, with plans to seek global regulatory approvals that could significantly enhance market opportunities and revenue potential.
  • Vaccine Development Support: Soligenix's Public Health Solutions segment includes the development of vaccines like RiVax®, supported by government grants from NIAID and BARDA, highlighting the company's strategic positioning and collaboration potential in the biodefense sector.
  • Future Outlook and Risks: Despite promising clinical trial results for HyBryte™, the company faces regulatory challenges from the FDA and EMA, indicating that future product development and commercialization efforts remain uncertain, necessitating close monitoring of market dynamics and policy changes.
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 -1.17, compared to its 5-year average forward P/E of -1.67. 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
-1.67
Current PE
-1.17
Overvalued PE
-0.28
Undervalued PE
-3.05

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
5Y Average PS
17.42
Current PS
38.19
Overvalued PS
30.14
Undervalued PS
4.71

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Frequently Asked Questions

What is Soligenix Inc (SNGX) stock price today?

The current price of SNGX is 1.26 USD — it has increased 2.44

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 -0.58 USD, decreased -25.64

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

Soligenix Inc (SNGX) has 14 emplpoyees as of March 18 2026.

What is Soligenix Inc (SNGX) market cap?

Today SNGX has the market capitalization of 12.71M USD.