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Voyager Therapeutics (VYGR)

(delayed data from nsdq).

-0.02 (-0.31%)

Updated Aug 16, 2024 04:00 PM ET

After-Market: $6.46 -0.01 (-0.15%) 7:58 PM ET

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Voyager Therapeutics, Inc. Stock

Us92915b1061, biotechnology & medical research, valuation: voyager therapeutics, inc., chart: voyager therapeutics, inc., latest news: voyager therapeutics, inc., last transcript: voyager therapeutics, inc..

Analysts' recommendations: Voyager Therapeutics, Inc.

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Etfs: voyager therapeutics, inc., other biotechnology & medical research, company profile.

Delayed Quote Nasdaq, August 16, 2024 at 04:00 pm EDT

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Buy Rating Affirmed for Voyager Therapeutics on Robust Pipeline and Strong Financial Position

Analyst Sumant Kulkarni of Canaccord Genuity maintained a Buy rating on Voyager Therapeutics ( VYGR – Research Report ), retaining the price target of $14.00.

Sumant Kulkarni has given his Buy rating due to a combination of factors surrounding Voyager Therapeutics’ promising developments in its pipeline. The company’s innovative approach includes an anti-tau antibody for Alzheimer’s disease and gene therapy programs for both Alzheimer’s and amyotrophic lateral sclerosis, leveraging their proprietary TRACER capsid platform. Kulkarni sees great potential in the tau-targeting strategies and gene therapy programs. Furthermore, the company’s TRACER technology is also encouraging external partnerships, indicating a positive outlook for the company’s collaborative efforts. Moreover, Kulkarni notes that while the visibility on the external programs is moderate, they seem to be advancing steadily. Voyager Therapeutics’ financial position, with enough funding to carry it into 2027, is considered strong, which could allow the company to continue its research and development efforts without immediate financial pressure. Looking ahead, a busy year is anticipated in 2025 with expected safety and pharmacokinetic data from Phase 1 studies and the filing of investigational new drug applications. These milestones could potentially drive the stock’s performance in the medium to long term, which supports the analyst’s Buy recommendation.

In another report released on August 8, Oppenheimer also maintained a Buy rating on the stock with a $18.00 price target.

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Voyager Therapeutics (VYGR) Company Description:

Voyager Therapeutics, Inc. operates as a clinical-stage gene therapy company, which develops treatments for patients suffering from central nervous system. Its pipeline of gene theraphy programs include VY-AADC, VY-SOD101, VY-HTT01, VY-FXN01, Tau Program, and VY-NAV01. The company was founded by Guangping Gao, Mark A. Kay, Krystof Bankiewicz and Phillip Zamore in June 2013 and is headquartered in Cambridge, MA.

Read More on VYGR:

• Voyager Therapeutics price target lowered to $7 from $8 at Wedbush
• Voyager Therapeutics to Present at Canaccord Genuity 44th Annual Growth Conference & Private Company Showcase
• Voyager Therapeutics reports Q2 EPS (18c), consensus (41c)
• Voyager Therapeutics Reports Second Quarter 2024 Financial and Operating Results
• VYGR Upcoming Earnings Report: What to Expect?

Voyager Therapeutics News MORE

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Theriva Biologics Announces Reverse Stock Split

ROCKVILLE, Md., Aug. 16, 2024 (GLOBE NEWSWIRE) — Theriva Biologics, Inc. (NYSE American: TOVX), a diversified clinical-stage company developing therapeutics designed to treat diseases in areas of high unmet need, announced today a reverse stock split of its issued and outstanding common stock, par value $0.001 per share, at a ratio of one (1) share of common stock for every twenty five (25) shares of common stock, effective as of 12:01 a.m. (Eastern Time) on August 26, 2024 (the “Effective Date”). The Company’s common stock will begin trading on a split-adjusted basis when the market opens on August 26, 2024. The reverse stock split was authorized by the Company’s Board of Directors on August 15, 2024. Pursuant to the laws of the State of Nevada, the Company’s state of incorporation, the Company’s Board of Directors has the authority to effect a reverse stock split without shareholder approval if the number of authorized shares of common stock and the number of outstanding shares of common stock are proportionally reduced. The Company will file a certificate of change to its articles of incorporation, as amended, with the Secretary of State of Nevada to effect the reverse stock split. The Company’s common stock will continue to trade on the NYSE American under the stock ticker “TOVX” but will trade under the new CUSIP number 87164U 508.

As a result of the reverse split, each twenty five (25) pre-split shares of common stock outstanding will automatically combine into one (1) new share of common stock without any action on the part of the holders, and the number of outstanding common shares will be reduced from 25,131,230 shares to 1,005,249 shares without taking into account fractional shares.

The reverse stock split is being effected to ensure that the Company can meet the per share price requirements of the NYSE American, the Company's current listing exchange.

No fractional shares will be issued as a result of the reverse stock split. Shareholders who otherwise would be entitled to a fractional share because they hold a number of shares not evenly divisible by the 1 (one) for twenty five (25) reverse split ratio, will automatically be entitled to receive an additional fractional share of the Company’s common stock to round up to the next whole share.

The Company’s transfer agent, Equiniti Trust Company, which is also acting as the exchange agent for the reverse split, will send instructions to stockholders of record who hold stock certificates regarding the exchange of their old certificates for new certificates, should they wish to do so. Stockholders who hold their shares in brokerage accounts or “street name” are not required to take action to effect the exchange of their shares.

About Theriva™ Biologics, Inc.

Theriva™ Biologics (NYSE American: TOVX), is a diversified clinical-stage company developing therapeutics designed to treat cancer and related diseases in areas of high unmet need. The Company is advancing a new oncolytic adenovirus platform designed for intravenous (IV), intravitreal and antitumoral delivery to trigger tumor cell death, improve access of co-administered cancer therapies to the tumor, and promote a robust and sustained anti-tumor response by the patient’s immune system. The Company’s lead candidates are: (1) VCN-01, an oncolytic adenovirus designed to replicate selectively and aggressively within tumor cells, and to degrade the tumor stroma barrier that serves as a significant physical and immunosuppressive barrier to cancer treatment; (2) SYN-004 (ribaxamase) which is designed to degrade certain commonly used IV beta-lactam antibiotics within the gastrointestinal (GI) tract to prevent microbiome damage, thereby limiting overgrowth of pathogenic organisms such as VRE (vancomycin resistant Enterococci) and reducing the incidence and severity of acute graft-versus-host-disease (aGVHD) in allogeneic hematopoietic cell transplant (HCT) recipients; and (3) SYN-020, a recombinant oral formulation of the enzyme intestinal alkaline phosphatase (IAP) produced under cGMP conditions and intended to treat both local GI and systemic diseases. For more information, please visit Theriva Biologics’ website at www.therivabio.com.

Forward-Looking Statement

This release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. In some cases forward-looking statements can be identified by terminology such as "may," "should," "potential," "continue," "expects," "anticipates," "intends," "plans," "believes," "estimates," and similar expressions, and include statements regarding our planned stock split. These forward-looking statements are based on management's expectations and assumptions as of the date of this press release and are subject to a number of risks and uncertainties, many of which are difficult to predict that could cause actual results to differ materially from current expectations and assumptions from those set forth or implied by any forward-looking statements. Important factors that could cause actual results to differ materially from current expectations include, among others, the stock split having the desired effect, t he ability to continue to enroll patients as planned, generating clinical data that establishes VCN-01 may lead to improved clinical outcomes for patients with PDAC and other solid cancers; the Company’s and VCN’s product candidates demonstrating safety and effectiveness, as well as results that are consistent with prior results; the ability to complete clinical trials on time and achieve the desired results and benefits; the ability to obtain regulatory approval for commercialization of product candidates or to comply with ongoing regulatory requirements, regulatory limitations relating to the Company’s and VCN’s ability to promote or commercialize their product candidates for the specific indications, acceptance of product candidates in the marketplace and the successful development, marketing or sale of the Company’s and VCN’s products, developments by competitors that render such products obsolete or non-competitive, the Company’s and VCN’s ability to maintain license agreements, the continued maintenance and growth of the Company’s and VCN’s patent estate, the ability to continue to remain well financed and other factors described in the Company’s Annual Report on Form 10-K for the year ended December 31, 2023 and its other filings with the SEC, including subsequent periodic reports on Forms 10-Q and current reports on Form 8-K. The information in this release is provided only as of the date of this release, and Theriva Biologics undertakes no obligation to update any forward-looking statements contained in this release on account of new information, future events, or otherwise, except as required by law.

For further information, please contact:

Investor Relations:

Chris Calabrese

LifeSci Advisors, LLC

[email protected] 

917-680-5608