Loading...

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

PDSB 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
0.680
Open
0.680
VWAP
0.66
Vol
200.21K
Mkt Cap
34.55M
Low
0.640
Amount
131.78K
EV/EBITDA(TTM)
--
Total Shares
52.83M
EV
27.63M
EV/OCF(TTM)
--
P/S(TTM)
--
PDS Biotechnology Corporation is a clinical-stage immunotherapy company. The Company is developing a pipeline of targeted cancer immunotherapies based on its Versamune T cell-activator and Versamune in combination with its interleukin 12 (IL-12) fused antibody drug conjugate (ADC), PDS01ADC, a tumor targeting immunocytokine. PDS0101 is its lead Versamune based immunotherapy. PDS0101 combines Versamune with a mixture of short proteins (peptides) derived from the cancer-causing HPV16 viral protein. Versamune is a proprietary lipid nanoparticle and T cell activating platform. PDS0301 is an investigational tumor-targeting antibody conjugate of Interleukin 12 (IL-12) that enhances the proliferation, potency, infiltration, and longevity of T cells in the tumor microenvironment. Its Versamune immunotherapies and Versamune in combination with PDS01ADC, are utilized for treatments in oncology, and Infectimune is utilized for preventive vaccines against infectious agents.
Show More

Events Timeline

(ET)
2026-02-20
08:40:00
PDS Biotechnology Amends VERSATILE-003 Clinical Trial Protocol
select
2026-01-28 (ET)
2026-01-28
09:00:00
PDS Biotechnology Presents PDS01ADC Study Results at AACR Conference
select
2026-01-22 (ET)
2026-01-22
08:50:00
PDS Biotechnology Receives Patent Allowance for PDS0101 Development
select
2026-01-09 (ET)
2026-01-09
08:50:00
PDS Biotechnology Submits Protocol Amendment for VERSATILE-003 Trial to FDA
select
2025-12-02 (ET)
2025-12-02
08:40:00
PDS Biotechnology Secures FDA Meeting to Discuss Accelerated Approval for PDS0101
select
2025-11-13 (ET)
2025-11-13
07:34:39
PDS Biotechnology announces Q3 earnings per share of 19 cents, below consensus estimate of 20 cents.
select
2025-11-11 (ET)
2025-11-11
15:34:26
PDS Biotechnology reveals registered direct offering of up to $11.1 million
select

News

Newsfilter
9.0
02-20Newsfilter
PDS Biotechnology Amends Phase 3 Trial Protocol for Accelerated Approval
  • Protocol Amendment: PDS Biotechnology Corporation announced an amendment to its Phase 3 VERSATILE-003 clinical trial protocol, adding progression-free survival (PFS) as an interim primary endpoint to support a potential accelerated approval pathway for PDS0101 in HPV16-positive recurrent and/or metastatic head and neck cancer.
  • Survival Endpoint Maintained: While PFS is added as an interim endpoint, the median overall survival (mOS) remains the primary endpoint, ensuring consistency with prior regulatory dialogues with the FDA, thereby enhancing the company's confidence in the regulatory approval process.
  • Accelerated Approval Potential: By including PFS as an interim primary endpoint, the trial duration is expected to shorten, accelerating the timeline for regulatory submission while improving cost efficiency, further advancing the company's strategic positioning in cancer immunotherapy.
  • Optimistic Market Outlook: PDS0101, as a targeted immunotherapy for HPV16-positive recurrent and/or metastatic head and neck cancer, developed in combination with standard immune checkpoint inhibitors, demonstrates strong market potential, aligning with the growing patient demand.
PRnewswire
8.5
01-12PRnewswire
Oncolytics Biotech Advances Pelareorep for Anal Cancer with 29% Response Rate
  • Clinical Data Breakthrough: Oncolytics Biotech's pelareorep demonstrated a 29% objective response rate in anal cancer during the GOBLET Cohort 4, significantly exceeding the historical benchmark of 10%, indicating its crucial clinical value in a setting with no FDA-approved treatment options.
  • Duration of Response: Among 14 evaluable patients, the median duration of response for pelareorep reached approximately 17 months, far surpassing the standard treatment's 9.5 months, showcasing the drug's durable efficacy in heavily pretreated patients and addressing a critical unmet medical need.
  • FDA Accelerated Approval Plans: Oncolytics plans to hold a Type C meeting with the FDA in Q1 2026 to discuss advancing pelareorep into a registration-directed clinical study, paving the way for potential accelerated approval if the data is validated.
  • Strategic Investment and Expert Support: The company expanded its Scientific Advisory Board by adding three globally recognized experts from Memorial Sloan Kettering Cancer Center and MD Anderson Cancer Center, further strengthening its strategic positioning in the gastrointestinal oncology field.
Newsfilter
8.5
01-12Newsfilter
Oncolytics Biotech Advances Pelareorep for Anal Cancer with 29% Response Rate
  • Clinical Data Breakthrough: Oncolytics Biotech's pelareorep demonstrated a 29% objective response rate in anal cancer patients during the GOBLET Cohort 4 study, significantly surpassing the historical benchmark of 10%, indicating the therapy's substantial potential in a patient population with no FDA-approved options.
  • Duration of Response: The study also revealed a median duration of response of approximately 17 months, far exceeding the standard treatment's 9.5 months, suggesting that pelareorep offers durable efficacy in heavily pretreated patients, addressing a critical unmet medical need.
  • FDA Accelerated Approval Plans: Oncolytics plans to hold a Type C meeting with the FDA in Q1 2026 to discuss advancing pelareorep into a registration-directed clinical study, paving the way for accelerated approval if the observed data can be replicated.
  • Strategic Investment and Expansion: The company is enhancing its strategic positioning in gastrointestinal oncology by expanding its Scientific Advisory Board, further solidifying its market presence in anal cancer and other indications.
Newsfilter
2.0
01-09Newsfilter
PDS Biotech Submits Amended Protocol for VERSATILE-003 Trial, Potentially Accelerating PDS0101 Approval
  • Clinical Trial Advancement: PDS Biotech has submitted an amended protocol to the FDA for the VERSATILE-003 trial, aiming to change the progression-free survival (PFS) endpoint to a primary measure, potentially accelerating the approval process for PDS0101 and enhancing the company's competitive position in cancer immunotherapy.
  • FDA Meeting Outcomes: The submission follows a constructive meeting with the FDA in December 2025, where the accelerated approval pathway for PDS0101 in HPV16-positive recurrent and/or metastatic head and neck cancer was discussed, reflecting strong communication with regulators and boosting investor confidence.
  • Clinical Data Support: Positive final results from the VERSATILE-002 trial provide data backing for this amendment, demonstrating promising median overall survival (mOS) and durable PFS, which may attract additional investment by validating the therapeutic potential of PDS0101.
  • Clear Strategic Goals: CEO Frank Bedu-Addo, PhD, stated that the amendment retains mOS and safety as requirements for full FDA approval while offering a significant opportunity to shorten the duration of VERSATILE-003, highlighting the company's long-term strategic positioning in cancer treatment.
NASDAQ.COM
4.0
2025-12-08NASDAQ.COM
PDS Biotechnology (PDSB) Receives Upgrade to Buy: Reasons Explained
  • Zacks Rank Upgrade: PDS Biotechnology (PDSB) has been upgraded to a Zacks Rank #2 (Buy), indicating a positive outlook on its earnings estimates, which are crucial for stock price movements.

  • Earnings Estimate Revisions: The Zacks Consensus Estimate for PDSB has increased by 9.4% over the past three months, reflecting analysts' growing confidence in the company's earnings potential.

  • Correlation with Stock Performance: There is a strong correlation between earnings estimate revisions and near-term stock movements, suggesting that PDSB's upgrade could lead to higher stock prices.

  • Zacks Rating System: The Zacks rating system maintains a balanced approach to stock ratings, with only the top 20% of stocks receiving a "Strong Buy" or "Buy" rating, positioning PDSB favorably for potential market-beating returns.

Newsfilter
9.0
2025-12-02Newsfilter
PDS Biotechnology Secures FDA Meeting to Discuss Accelerated Approval for PDS0101
  • FDA Meeting Approval: PDS Biotechnology's request for a Type C meeting with the FDA has been accepted, scheduled for this month to discuss the accelerated approval pathway for PDS0101 in HPV16-positive recurrent head and neck cancer, marking a significant advancement in the company's cancer immunotherapy efforts.
  • Clinical Trial Results: The final results from the VERSATILE-002 trial demonstrated promising median overall survival and durable progression-free survival, providing data support for the accelerated approval of PDS0101, potentially shortening the regulatory approval timeline.
  • Trial Design Change: The company plans to amend the VERSATILE-003 Phase 3 trial to change the progression-free survival endpoint to a surrogate primary endpoint that can be evaluated earlier, enhancing statistical power and laying the groundwork for accelerated approval, thereby increasing market competitiveness.
  • Strategic Outlook: PDS Biotechnology's CEO stated that the positive progression-free survival data offers a crucial opportunity to shorten the duration to a primary endpoint, which is expected to expedite treatment availability, meet patient needs, and enhance the company's position in the cancer treatment market.
Wall Street analysts forecast PDSB stock price to rise
2 Analyst Rating
Wall Street analysts forecast PDSB stock price to rise
2 Buy
0 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
3.00
Averages
9.00
High
15.00
Current: 0.000
sliders
Low
3.00
Averages
9.00
High
15.00
B. Riley
Buy
downgrade
$5 -> $3
AI Analysis
2025-11-25
Reason
B. Riley
Price Target
$5 -> $3
AI Analysis
2025-11-25
downgrade
Buy
Reason
B. Riley lowered the firm's price target on PDS Biotechnology to $3 from $5 and keeps a Buy rating on the shares. The shares remain attractively valued with near-zero EV that fails to reflect impact of this recent strategic pivot on enrollment size, efficacy endpoint durations and an enriched p16+ve population with limited competing trials, the analyst tells investors in a research note.
H.C. Wainwright
Buy
maintain
$13 -> $15
2025-11-13
Reason
H.C. Wainwright
Price Target
$13 -> $15
2025-11-13
maintain
Buy
Reason
H.C. Wainwright raised the firm's price target on PDS Biotechnology to $15 from $13 and keeps a Buy rating on the shares. The firm is increasing its view of the probability of success for PDS0101 in head and neck cancer to 65% from 40% following the most recent median overall survival data from the VERSATILE-002 study, the analyst tells investors.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for PDSB
Unlock Now

Valuation Metrics

The current forward P/E ratio for PDS Biotechnology Corp (PDSB.O) is -1.14, compared to its 5-year average forward P/E of -4.78. For a more detailed relative valuation and DCF analysis to assess PDS Biotechnology Corp'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
-4.78
Current PE
-1.14
Overvalued PE
-0.38
Undervalued PE
-9.18

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
-3.56
Current EV/EBITDA
-0.97
Overvalued EV/EBITDA
0.27
Undervalued EV/EBITDA
-7.40

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
89.46
Current PS
0.00
Overvalued PS
472.28
Undervalued PS
-293.35

Financials

AI Analysis
Annual
Quarterly

Whales Holding PDSB

Trading Trends

    Insider
    Hedge Fund
    Congress Trading

People Also Watch

Frequently Asked Questions

What is PDS Biotechnology Corp (PDSB) stock price today?

The current price of PDSB is 0.654 USD — it has decreased -4.53

What is PDS Biotechnology Corp (PDSB)'s business?

PDS Biotechnology Corporation is a clinical-stage immunotherapy company. The Company is developing a pipeline of targeted cancer immunotherapies based on its Versamune T cell-activator and Versamune in combination with its interleukin 12 (IL-12) fused antibody drug conjugate (ADC), PDS01ADC, a tumor targeting immunocytokine. PDS0101 is its lead Versamune based immunotherapy. PDS0101 combines Versamune with a mixture of short proteins (peptides) derived from the cancer-causing HPV16 viral protein. Versamune is a proprietary lipid nanoparticle and T cell activating platform. PDS0301 is an investigational tumor-targeting antibody conjugate of Interleukin 12 (IL-12) that enhances the proliferation, potency, infiltration, and longevity of T cells in the tumor microenvironment. Its Versamune immunotherapies and Versamune in combination with PDS01ADC, are utilized for treatments in oncology, and Infectimune is utilized for preventive vaccines against infectious agents.

What is the price predicton of PDSB Stock?

Wall Street analysts forecast PDSB stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for PDSB is9.00 USD with a low forecast of 3.00 USD and a high forecast of 15.00 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 PDS Biotechnology Corp (PDSB)'s revenue for the last quarter?

PDS Biotechnology Corp revenue for the last quarter amounts to -8.14M USD, decreased -20.03

What is PDS Biotechnology Corp (PDSB)'s earnings per share (EPS) for the last quarter?

PDS Biotechnology Corp. EPS for the last quarter amounts to -5916048.00 USD, decreased -26.05

How many employees does PDS Biotechnology Corp (PDSB). have?

PDS Biotechnology Corp (PDSB) has 24 emplpoyees as of March 13 2026.

What is PDS Biotechnology Corp (PDSB) market cap?

Today PDSB has the market capitalization of 34.55M USD.