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Grace Therapeutics (formerly Acasti Pharma)

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Namestring
Grace Therapeutics (formerly Acasti Pharma)
Legal namestring
Grace Therapeutics, Inc.
Websiteurl
gracetx.com
Company typeenum
Public
Founded yearint
2012
Descriptiontext

Grace Therapeutics, Inc. (NASDAQ: GRCE) is a late-stage clinical biopharmaceutical company developing drug candidates for rare and orphan diseases, with its headquarters in Princeton, New Jersey. The company's core technology is a proprietary nanoparticle platform that enables aqueous formulation of otherwise insoluble drugs for standard peripheral IV infusion. Its lead asset, GTx-104, is a novel IV formulation of nimodipine in development for aneurysmal subarachnoid hemorrhage (aSAH), a rare and life-threatening neurological emergency affecting approximately 50,000 patients per year in the United States. GTx-104 has received FDA Orphan Drug Designation, providing seven years of marketing exclusivity upon approval, and is protected by over 40 granted and pending patents worldwide.

The company targets acute care hospitals and neurocritical care centers as its primary customer segment, with specialist neurologists and neurosurgeons as key prescribing personas. Following the April 2026 FDA Complete Response Letter citing CMC concerns (leachables data, toxicology risk assessments, and manufacturing deficiencies at the contract manufacturer), the company plans to request a Type A meeting with the FDA. The pivotal STRIVE-ON Phase 3 trial met its primary endpoint with a 19% reduction in clinically significant hypotension versus oral nimodipine, supporting the clinical differentiation case for IV delivery in critically ill aSAH patients.

Grace Therapeutics is currently pre-revenue, with planned monetization through pharmaceutical product sales to hospital formularies and specialty healthcare providers post-approval, with potential premium pricing enabled by orphan drug status. The company was created through Acasti Pharma's August 2021 all-stock acquisition of Grace Therapeutics Inc. for approximately $138 million, after which the combined entity rebranded from Acasti Pharma back to the original Grace Therapeutics name. The pipeline also includes GTX-102 and GTX-101, both with Orphan Drug Designation. The company has funded operations through multiple private placements including $7.5M in September 2023, $10.46M in February 2025, and additional warrant exercises of approximately $4M and $2.86M in October 2025.

Short descriptiontext

Grace Therapeutics is a late-stage clinical biopharmaceutical company developing GTx-104, a novel IV nanoparticle formulation of nimodipine for aneurysmal subarachnoid hemorrhage, targeting acute care hospitals and neurocritical care specialists with FDA Orphan Drug Designation providing seven years of marketing exclusivity.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLaval, Canada
HQ citystring
Laval
HQ countrystring
Canada
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
intravenous drug delivery, rare disease therapeutics, subarachnoid hemorrhage treatment, nanoparticle drug formulation, orphan drug development
Industry3 codes
1Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryYes
2Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryNo
3Rare Cardiovascular & Vascular Disorder Therapies
CodeHLAIAIAHPrimaryNo
NAICS code2 codes
  • Medicinal and Botanical Manufacturing325411
  • Scientific Research and Development Services5417
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Pharmaceuticals (Neurocritical Care)
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Sales
TypeOne Time License
Description

Post FDA approval, Grace Therapeutics will generate revenue through sales of GTx-104 to hospitals and healthcare providers for treatment of aneurysmal subarachnoid hemorrhage. Revenue will come from product sales with potential for premium pricing due to orphan drug designation and competitive differentiation.

gracetx.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Operations, Personnel, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Grace Therapeutics develops and is preparing to commercialize GTx-104, a clinical-stage, novel injectable (IV) formulation of nimodipine enabled by proprietary nanoparticle technology that allows aqueous solubilization of the otherwise insoluble drug for peripheral IV infusion in aneurysmal subarachnoid hemorrhage (aSAH) patients. The pipeline also includes additional rare/orphan neurology candidates (GTX-102, GTX-101) protected by a 40+ patent portfolio and FDA Orphan Drug Designation.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Grace Therapeutics is a late-stage biopharma company developing drug candidates that target rare and orphan diseases. The company's lead clinical asset is GTx-104, an intravenous infusion formulation of nimodipine targeting aneurysmal subarachnoid hemorrhage (aSAH), a rare and life-threatening medical emergency. Grace Therapeutics' novel drug delivery technologies have the potential to improve the performance of currently marketed drugs through nanoparticle technology that enables improved bioavailability and patient management. The company also has additional pipeline candidates (GTX-102, GTX-101) and holds over 40 granted and pending patents with Orphan Drug Designation from the FDA providing seven years of marketing exclusivity.

Product and service1 record
1GTx-104
CategorySpecialty Pharmaceuticals / Neurology (aSAH)
Description

Clinical-stage, novel injectable (IV) formulation of nimodipine enabled by proprietary nanoparticle technology that solubilizes the otherwise insoluble dihydropyridine calcium channel blocker for standard peripheral IV infusion in aneurysmal subarachnoid hemorrhage (aSAH) patients. Designed for neurocritical care specialists, ICU pharmacists, and hospital formularies treating aSAH patients, including those who are unconscious or dysphagic and cannot take oral medication.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Late-stage CNS-focused biopharma developing novel therapies for rare and serious neurological conditions. Comparable in focusing on CNS specialty indications with high unmet need and orphan drug positioning.

TypeDirect peer
Description

Former direct peer developing EG-1962 (nimodipine microparticles) for aSAH; Grace's current CMO Dr. Macdonald was previously CSO there. Failed Phase 3 NEWTON trial but represents the closest historical comparable in the aSAH drug-delivery space.

TypeDirect peer
Description

Specialty pharma focused on rare and orphan diseases with reformulated/improved versions of established molecules. Comparable business model of developing niche, differentiated formulations for underserved patient populations.

TypeBroad incumbent
Description

Specialty neurology biopharma developing differentiated therapies for CNS disorders. Comparable in CNS-focused drug development with orphan and specialty positioning, though broader in scale.

TypeBroad incumbent
Description

Markets generic nimodipine oral capsules in the US and is a major specialty pharma player. Directly competes with GTx-104 as a low-cost nimodipine supplier to hospitals treating aSAH patients.

TypeBroad incumbent
Description

Generic and specialty pharmaceutical company with a portfolio including nimodipine products and broader neurology offerings. Comparable in providing nimodipine alternatives and competing in neurocritical care channels.

TypeDirect peer
Description

Clinical-stage biopharma focused on immuno-neurology and rare neurological disorders with reformulated/innovative therapies. Comparable in CNS specialty pharma positioning, small-cap profile, and orphan/rare disease strategy.

TypeDirect peer
Description

Specialty pharma focused on neurology and rare disease products with reformulation/improved-delivery strategies. Comparable in targeting underserved specialty indications with differentiated drug-delivery approaches.

TypeBroad incumbent
Description

Specialty pharma division with strong neurology portfolio. While broader than Grace, it competes in neurocritical care and rare CNS indications, making it a relevant incumbent comparable for hospital-channel specialty products.

TypeBroad incumbent
Description

Markets Nimotop, the original oral nimodipine brand approved for aSAH. While a broad pharma incumbent, it competes head-to-head with GTx-104 in the same clinical indication and sets the existing standard-of-care benchmark.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles4 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds11 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors3 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Grace Therapeutics (formerly Acasti Pharma)

Specialty Pharmaceuticals (Neurocritical Care)gracetx.com

Grace Therapeutics is a late-stage clinical biopharmaceutical company developing GTx-104, a novel IV nanoparticle formulation of nimodipine for aneurysmal subarachnoid hemorrhage, targeting acute care hospitals and neurocritical care specialists with FDA Orphan Drug Designation providing seven years of marketing exclusivity.

What Grace Therapeutics (formerly Acasti Pharma) does

Grace Therapeutics, Inc. (NASDAQ: GRCE) is a late-stage clinical biopharmaceutical company developing drug candidates for rare and orphan diseases, with its headquarters in Princeton, New Jersey. The company's core technology is a proprietary nanoparticle platform that enables aqueous formulation of otherwise insoluble drugs for standard peripheral IV infusion. Its lead asset, GTx-104, is a novel IV formulation of nimodipine in development for aneurysmal subarachnoid hemorrhage (aSAH), a rare and life-threatening neurological emergency affecting approximately 50,000 patients per year in the United States. GTx-104 has received FDA Orphan Drug Designation, providing seven years of marketing exclusivity upon approval, and is protected by over 40 granted and pending patents worldwide.

The company targets acute care hospitals and neurocritical care centers as its primary customer segment, with specialist neurologists and neurosurgeons as key prescribing personas. Following the April 2026 FDA Complete Response Letter citing CMC concerns (leachables data, toxicology risk assessments, and manufacturing deficiencies at the contract manufacturer), the company plans to request a Type A meeting with the FDA. The pivotal STRIVE-ON Phase 3 trial met its primary endpoint with a 19% reduction in clinically significant hypotension versus oral nimodipine, supporting the clinical differentiation case for IV delivery in critically ill aSAH patients.

Grace Therapeutics is currently pre-revenue, with planned monetization through pharmaceutical product sales to hospital formularies and specialty healthcare providers post-approval, with potential premium pricing enabled by orphan drug status. The company was created through Acasti Pharma's August 2021 all-stock acquisition of Grace Therapeutics Inc. for approximately $138 million, after which the combined entity rebranded from Acasti Pharma back to the original Grace Therapeutics name. The pipeline also includes GTX-102 and GTX-101, both with Orphan Drug Designation. The company has funded operations through multiple private placements including $7.5M in September 2023, $10.46M in February 2025, and additional warrant exercises of approximately $4M and $2.86M in October 2025.

Grace Therapeutics (formerly Acasti Pharma) firmographics

Firmographics
Name
Grace Therapeutics (formerly Acasti Pharma)
Legal name
Grace Therapeutics, Inc.
Website
https://gracetx.com
Company type
Public
Founded year
2012
Operating status
Operating
Headcount range
11–50 employees
Short description
Grace Therapeutics is a late-stage clinical biopharmaceutical company developing GTx-104, a novel IV nanoparticle formulation of nimodipine for aneurysmal subarachnoid hemorrhage, targeting acute care hospitals and neurocritical care specialists with FDA Orphan Drug Designation providing seven years of marketing exclusivity.
Ownership category
akta.pro rank

Grace Therapeutics (formerly Acasti Pharma) industry classification

Industry
Product category
Specialty Pharmaceuticals (Neurocritical Care)
NAICS
Medicinal and Botanical Manufacturing (325411), Scientific Research and Development Services (5417)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)
akta.pro secondary industries
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF), Rare Cardiovascular & Vascular Disorder Therapies (HLAIAIAH)

Keywords

  • Intravenous drug delivery
  • Rare disease therapeutics
  • Subarachnoid hemorrhage treatment
  • Nanoparticle drug formulation
  • Orphan drug development

Where Grace Therapeutics (formerly Acasti Pharma) is headquartered

Location

Headquarters

HQ city
Laval
HQ country
Canada
HQ region
North America

Offices2 records

Markets served

Grace Therapeutics (formerly Acasti Pharma) business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Operations, Personnel, Marketing or Sales

Revenue model

  1. Pharmaceutical Product Sales: Post FDA approval, Grace Therapeutics will generate revenue through sales of GTx-104 to hospitals and healthcare providers for treatment of aneurysmal subarachnoid hemorrhage. Revenue will come from product sales with potential for premium pricing due to orphan drug designation and competitive differentiation.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Grace Therapeutics (formerly Acasti Pharma) product offering

Product offering

Core offering

Grace Therapeutics develops and is preparing to commercialize GTx-104, a clinical-stage, novel injectable (IV) formulation of nimodipine enabled by proprietary nanoparticle technology that allows aqueous solubilization of the otherwise insoluble drug for peripheral IV infusion in aneurysmal subarachnoid hemorrhage (aSAH) patients. The pipeline also includes additional rare/orphan neurology candidates (GTX-102, GTX-101) protected by a 40+ patent portfolio and FDA Orphan Drug Designation.

Product overview

Grace Therapeutics is a late-stage biopharma company developing drug candidates that target rare and orphan diseases. The company's lead clinical asset is GTx-104, an intravenous infusion formulation of nimodipine targeting aneurysmal subarachnoid hemorrhage (aSAH), a rare and life-threatening medical emergency. Grace Therapeutics' novel drug delivery technologies have the potential to improve the performance of currently marketed drugs through nanoparticle technology that enables improved bioavailability and patient management. The company also has additional pipeline candidates (GTX-102, GTX-101) and holds over 40 granted and pending patents with Orphan Drug Designation from the FDA providing seven years of marketing exclusivity.

Differentiator

Problem solved

Functional benefit

Products and services

  • GTx-104 Clinical-stage, novel injectable (IV) formulation of nimodipine enabled by proprietary nanoparticle technology that solubilizes the otherwise insoluble dihydropyridine calcium channel blocker for standard peripheral IV infusion in aneurysmal subarachnoid hemorrhage (aSAH) patients. Designed for neurocritical care specialists, ICU pharmacists, and hospital formularies treating aSAH patients, including those who are unconscious or dysphagic and cannot take oral medication.

Companies that use Grace Therapeutics (formerly Acasti Pharma)

Customer profile

Segments2 records

Ideal customer profiles2 records

Grace Therapeutics (formerly Acasti Pharma) technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Grace Therapeutics (formerly Acasti Pharma) partnerships and signals

Strategic signal

Scale indicators8 records

Recent moves7 records

Expansion highlights4 records

Grace Therapeutics (formerly Acasti Pharma) competitors and assessment

Company assessment

Direct peers

  • Sage Therapeutics: Late-stage CNS-focused biopharma developing novel therapies for rare and serious neurological conditions. Comparable in focusing on CNS specialty indications with high unmet need and orphan drug positioning.
  • Edge Therapeutics: Former direct peer developing EG-1962 (nimodipine microparticles) for aSAH; Grace's current CMO Dr. Macdonald was previously CSO there. Failed Phase 3 NEWTON trial but represents the closest historical comparable in the aSAH drug-delivery space.
  • Azurity Pharmaceuticals: Specialty pharma focused on rare and orphan diseases with reformulated/improved versions of established molecules. Comparable business model of developing niche, differentiated formulations for underserved patient populations.
  • BioXcel Therapeutics: Clinical-stage biopharma focused on immuno-neurology and rare neurological disorders with reformulated/innovative therapies. Comparable in CNS specialty pharma positioning, small-cap profile, and orphan/rare disease strategy.
  • Assertio Therapeutics: Specialty pharma focused on neurology and rare disease products with reformulation/improved-delivery strategies. Comparable in targeting underserved specialty indications with differentiated drug-delivery approaches.

Broad incumbents

  • Cerevel Therapeutics: Specialty neurology biopharma developing differentiated therapies for CNS disorders. Comparable in CNS-focused drug development with orphan and specialty positioning, though broader in scale.
  • Mallinckrodt Pharmaceuticals: Markets generic nimodipine oral capsules in the US and is a major specialty pharma player. Directly competes with GTx-104 as a low-cost nimodipine supplier to hospitals treating aSAH patients.
  • Amneal Pharmaceuticals: Generic and specialty pharmaceutical company with a portfolio including nimodipine products and broader neurology offerings. Comparable in providing nimodipine alternatives and competing in neurocritical care channels.
  • Merz Therapeutics: Specialty pharma division with strong neurology portfolio. While broader than Grace, it competes in neurocritical care and rare CNS indications, making it a relevant incumbent comparable for hospital-channel specialty products.
  • Pfizer (Nimotop): Markets Nimotop, the original oral nimodipine brand approved for aSAH. While a broad pharma incumbent, it competes head-to-head with GTx-104 in the same clinical indication and sets the existing standard-of-care benchmark.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Grace Therapeutics (formerly Acasti Pharma) social profiles

Digital presence

Grace Therapeutics (formerly Acasti Pharma) financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Grace Therapeutics (formerly Acasti Pharma) leadership team

Management profile

Number of profiles

Profiles4 records

Grace Therapeutics (formerly Acasti Pharma) subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Grace Therapeutics (formerly Acasti Pharma) funding detail

Funding detail

Funding overview

Funding rounds11 records

Investors3 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Grace Therapeutics (formerly Acasti Pharma) M&A and investment

M&A and investment

M&A1 record

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Grace Therapeutics (formerly Acasti Pharma)

What does Grace Therapeutics (formerly Acasti Pharma) do?

Grace Therapeutics develops and is preparing to commercialize GTx-104, a clinical-stage, novel injectable (IV) formulation of nimodipine enabled by proprietary nanoparticle technology that allows aqueous solubilization of the otherwise insoluble drug for peripheral IV infusion in aneurysmal subarachnoid hemorrhage (aSAH) patients. The pipeline also includes additional rare/orphan neurology candidates (GTX-102, GTX-101) protected by a 40+ patent portfolio and FDA Orphan Drug Designation.

Is Grace Therapeutics (formerly Acasti Pharma) a public or private company?

Grace Therapeutics (formerly Acasti Pharma) is a public company. It is classified as public and is currently operating.

When was Grace Therapeutics (formerly Acasti Pharma) founded?

Grace Therapeutics (formerly Acasti Pharma) was founded in 2012. It employs 11 to 50 people.

Where is Grace Therapeutics (formerly Acasti Pharma) based?

Grace Therapeutics (formerly Acasti Pharma) is headquartered in Laval, Canada, in the North America region.

How does Grace Therapeutics (formerly Acasti Pharma) make money?

One revenue line is on record: pharmaceutical Product Sales.

Who are Grace Therapeutics (formerly Acasti Pharma)'s main competitors?

Direct peers on record are Sage Therapeutics, Edge Therapeutics, Azurity Pharmaceuticals, BioXcel Therapeutics and Assertio Therapeutics. Broad incumbents are Cerevel Therapeutics, Mallinckrodt Pharmaceuticals, Amneal Pharmaceuticals, Merz Therapeutics and Pfizer (Nimotop).

Does Grace Therapeutics (formerly Acasti Pharma) have an API?

No public API is recorded for Grace Therapeutics (formerly Acasti Pharma).

What industry is Grace Therapeutics (formerly Acasti Pharma) in?

Grace Therapeutics (formerly Acasti Pharma)'s product category is Specialty Pharmaceuticals (Neurocritical Care). Its primary akta.pro industry code is HLAIACAC, Neurology & CNS Specialty Pharmaceuticals, with a secondary code of HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals. Its NAICS code is 325411 and its SIC code is 2834.

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Live signals
Ticker ReportGrace Therapeutics (NASDAQ:GRCE) Downgraded by Wall Street Zen to Strong SellWall Street Zen downgraded Grace Therapeutics to a strong sell rating. The company reported Q2 EPS of -$0.91, missing the -$0.13 consensus, and analysts forecast -$0.80 for the year. The stock opened at $2.07 with a consensus target of $6.00.Defense WorldBank of America Corp DE Makes New Investment in Grace Therapeutics, Inc. $GRCEBank of America Corp DE acquired a new stake in Grace Therapeutics, purchasing 494,698 shares worth about $1.123 million in Q2. The fund now holds roughly 2.35% of the company, and other institutions also added positions. Grace Therapeutics reported a Q2 loss of $0.91 per share, missing estimates.American Banking and Market News494,698 Shares in Grace Therapeutics, Inc. $GRCE Acquired by Bank of America Corp DEBank of America Corp DE acquired a new stake in Grace Therapeutics, purchasing 494,698 shares valued at approximately $1,123,000 in Q2. Other hedge funds also adjusted positions, and analysts rate the stock a Hold with a $6.00 price target. The company reported a Q2 loss of $0.91 per share, missing estimates.The future of tradingOpaleye Management reports $16,404 Grace Therapeutics common share purchaseOpaleye Management, a 10% owner of Grace Therapeutics, bought 7,849 common shares at $2.09. The purchase raised its indirect stake through Opaleye, L.P. to 2,798,167 shares.Ticker ReportGrace Therapeutics (NASDAQ:GRCE) Stock Bumped Up to Sell by Wall Street ZenWall Street Zen upgraded Grace Therapeutics from strong sell to sell, while Zacks raised it to hold. The company reported Q2 EPS of -$0.91, missing the -$0.13 consensus, and institutional investors own 6.08% of the stock.The future of tradingOpaleye Management reports $31,687 Grace Therapeutics common share purchaseOpaleye Management raised its stake in Grace Therapeutics to 2,855,318 shares, held indirectly through Opaleye, L.P. The fund bought 15,089 shares at $2.1 each in open-market purchases.NasdaqThursday 9/10 Insider Buying Report: SEI, GRCEAJ Teague, director of Solaris Energy Infrastructure, bought 7,800 SEI shares for $500,994 on Tuesday. Prashant Kohli, CEO of Grace Therapeutics, bought 100,000 GRCE shares for $214,000 on Wednesday. Both purchases were filed as insider buys.Stock TitanGrace Therapeutics to Present at H.C. WainwrightGrace Therapeutics CEO Prashant Kohli will present on its lead asset GTx-104 for aneurysmal subarachnoid hemorrhage at the H.C. Wainwright 28th Annual Global Investment Conference in New York, September 14-16, 2026. The presentation will be available on demand from September 11, and investors can arrange one-on-one meetings.Quiver QuantitativeGrace Therapeutics Announces $10 Million Private Placement Financing to Support GTx-104 Development | GRCE Stock NewsGrace Therapeutics, Inc. announced a $10 million private placement financing involving the issuance of 4,761,904 shares at $2.10 per share, expected to close on August 6, 2026. The proceeds will fund manufacturing and regulatory work for GTx-104, an injectable nimodipine formulation for aneurysmal subarachnoid hemorrhage, extending the company's cash runway to late 2028. The company is also implementing a dual-source manufacturing strategy to address FDA compliance issues with its current contract manufacturer, with a technology transfer to a second U.S.-based manufacturer already underway.Investing.comGrace Therapeutics raises $10 million in private placement By Investing.comGrace Therapeutics, Inc. announced it has entered into a securities purchase agreement for a private placement financing expected to generate approximately $10 million in gross proceeds by issuing 4,761,904 shares of common stock at $2.10 per share to new and existing investors, with closing expected on August 6, 2026. The company intends to use the net proceeds to support manufacturing and regulatory work for GTx-104, its injectable nimodipine candidate for aneurysmal subarachnoid hemorrhage, which combined with existing cash extends its runway through the end of calendar 2028. Grace Therapeutics has also initiated a dual-source manufacturing strategy with a technology transfer to a U.S.-based contract manufacturer underway, making manufacturing readiness the key driver of NDA resubmission timing.