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Imvax

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uuid0000upr

Namestring
Imvax
Legal namestring
Imvax, Inc.
Websiteurl
imvax.com
Company typeenum
Private
Founded yearint
2015
Descriptiontext

Imvax is a privately held, clinical-stage biotechnology company founded in 2015 and headquartered in Philadelphia, PA, that develops personalized, whole tumor-derived immunotherapies for solid tumors. The company is built around its proprietary Goldspire® platform, which captures a patient's full tumor antigen signature by combining resected tumor cells with an antisense oligodeoxynucleotide (IMV-001) targeting insulin-like growth factor type 1 receptor (IGF-1R) inside proprietary implantable biodiffusion chambers (BDCs). Tumor samples are processed at Imvax's Philadelphia manufacturing facility in under 24 hours, loaded into BDCs, irradiated, and returned to the hospital for implantation in the patient's abdomen for approximately 48 hours, during which immunogenic cell death releases antigens that stimulate both innate and adaptive immunity.

The lead clinical candidate is IGV-001, an autologous biologic-device combination product for newly diagnosed glioblastoma multiforme (ndGBM), which has received both FDA Fast Track and Orphan Drug Designations. In December 2025, Imvax reported positive Phase 2b top-line data showing median overall survival of 20.3 months versus 14.0 months for placebo (+45% improvement), although the primary progression-free survival endpoint was not met. Approximately 99 patients were enrolled across 19-20 U.S. academic medical centers. The pipeline extends the Goldspire® platform to additional solid tumors, with IHC-001 (hepatocellular carcinoma), IUC-001 (urothelial cancer), IOC-001 (ovarian cancer), and IEC-001 (endometrial cancer) in preclinical or IND-enabling stages.

Imvax has no approved products and no commercial revenue. The company is funded entirely through private capital, having raised approximately $86 million across three rounds between September 2023 and January 2025 from existing and new investors. Distribution of its investigational therapies is exclusively through clinical trial enrollment at major U.S. academic cancer centers. The company is led by Executive Chairman John P. Furey (formerly COO of Spark Therapeutics where he launched LUXTURNA), COO Sean P. Hemingway (formerly Global Head of BioLife Plasma Services at Takeda), and CFO/CLO John M. Limongelli, signaling operational and commercial readiness rather than further research scaling.

Short descriptiontext

Imvax is a privately held, clinical-stage Philadelphia biotech developing personalized whole-tumor immunotherapies via its proprietary Goldspire® platform, with lead candidate IGV-001 in Phase 2b for newly diagnosed glioblastoma and pipeline programs across multiple solid tumors.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersPhiladelphia, United States
HQ citystring
Philadelphia
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
personalized cancer immunotherapy, autologous cell therapy, glioblastoma treatment, tumor-derived vaccines, biologic-device combinations
Industry4 codes
1Cell Therapy Developers (Autologous)
CodeHLAAABAAPrimaryYes
2Therapeutic Vaccines (e.g., Cancer/Chronic Infection)
CodeHLAIAEAGPrimaryNo
3Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies)
CodeHLAAANAKPrimaryNo
4Therapeutic Vaccines (cancer, chronic infection immunotherapy)
CodeHLAAAEABPrimaryNo
NAICS code1 code
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Personalized Cancer Immunotherapy
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pre-revenue / Clinical Stage Development
TypeOne Time License
Description

Imvax is a clinical-stage biotechnology company with no approved products or commercial revenue. The company is developing personalized immunotherapies for solid tumors, with its lead candidate IGV-001 in Phase 2b clinical development for newly diagnosed glioblastoma. Revenue will depend on successful clinical development, regulatory approval, and commercialization of its pipeline products.

imvax.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 components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1Goldspire®
Description

Imvax's proprietary immunotherapy platform that delivers personalized, whole tumor-derived immunotherapies by capturing a tumor's full antigen signature and using it to stimulate the patient's innate and adaptive immunity.

imvax.com
Core offering1 text field

Imvax develops personalized, whole tumor-derived autologous immunotherapies through its proprietary Goldspire® platform. The platform combines patient-derived tumor cells with antisense oligodeoxynucleotide IMV-001 against IGF-1R, loaded into implantable biodiffusion chambers (BDCs), to deliver a full tumor antigen payload and stimulate both innate and adaptive immune responses against residual tumor cells. The lead candidate IGV-001, an autologous biologic-device combination product for newly diagnosed glioblastoma, has reported positive Phase 2b results with median overall survival of 20.3 months versus 14.0 months for placebo.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Phase 2b trial: Median OS of 20.3 months vs 14.0 months placebo (+45% improvement)
+3 more records
Product overview1 text field

Imvax is a clinical-stage biotechnology company with a platform-plus-products architecture. The core technology is the Goldspire® platform, a personalized, whole tumor-derived immunotherapy that combines patient-derived tumor cells with an antisense oligonucleotide (IMV-001) delivered via proprietary biodiffusion chambers. The lead product is IGV-001 for newly diagnosed glioblastoma, which has completed Phase 2b trials and received FDA Fast Track designation. The pipeline includes multiple programs (IHC-001 for hepatocellular carcinoma, IUC-001 for urothelial cancer, IOC-001 for ovarian cancer, IEC-001 for endometrial cancer, and ICC-001) at various stages from IND-enabling to preclinical studies, all leveraging the same Goldspire® platform technology.

Product and service5 records
1IGV-001
CategoryLead Clinical-Stage Product Candidate
Description

Autologous biologic-device combination product candidate derived from the Goldspire® platform for the treatment of newly diagnosed glioblastoma (ndGBM). Combines patient-derived tumor cells with antisense oligodeoxynucleotide IMV-001 loaded into proprietary biodiffusion chambers implanted for approximately 48 hours. FDA Fast Track Designation and Orphan Drug Designation granted; Phase 2b top-line results announced December 2025 showed median overall survival of 20.3 months versus 14.0 months for placebo (+45%) with no drug-related serious adverse events.

2IHC-001
CategoryPipeline Product Candidate
Description

Pipeline product candidate for hepatocellular carcinoma (primary liver cancer) being developed using the Goldspire® platform. Preclinical studies are ongoing.

3IUC-001
CategoryPipeline Product Candidate
Description

Pipeline product candidate for urothelial (bladder) cancer being developed using the Goldspire® platform. Preclinical studies are ongoing.

4IOC-001
CategoryPipeline Product Candidate
Description

Pipeline product candidate for ovarian cancer being developed using the Goldspire® platform. Preclinical studies are ongoing.

5IEC-001
CategoryPipeline Product Candidate
Description

Pipeline product candidate for endometrial cancer being developed using the Goldspire® platform. Currently in IND-enabling stage.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Develops engineered autologous TCR-T cell therapies for solid tumors. Comparable cell therapy modality and oncology focus to Imvax's Goldspire platform.

TypeDirect peer
Description

Pioneer in tumor-infiltrating lymphocyte (TIL) autologous cell therapy, with an FDA-approved product (Amtagvi) in solid tumors. Comparable as a commercial-stage autologous cell therapy developer in oncology.

TypeEmerging player
Description

Develops viral immunotherapies and autologous cancer vaccines including CAN-3110 for glioblastoma. Adjacent modality but competing in the same indication as Imvax.

TypeDirect peer
Description

Clinical-stage cell and gene therapy company developing autologous and allogeneic therapies for oncology, including CAR-T programs for solid tumors and hematologic malignancies.

TypeDirect peer
Description

Develops cell and gene therapies for solid tumors, including autologous CAR-T programs for GBM. Comparable as a clinical-stage personalized cell therapy developer targeting brain tumors.

TypeBroad incumbent
Description

Large immuno-oncology incumbent with Opdivo (nivolumab) and a broad oncology pipeline. Relevant as a potential strategic acquirer of cell therapy assets like Imvax's IGV-001.

TypeDirect peer
Description

Developer of DCVax-L, an autologous dendritic cell vaccine for glioblastoma. Closely comparable as both companies pursue personalized cell-based immunotherapy approaches for newly diagnosed GBM.

TypeDirect peer
Description

Develops autologous dendritic cell vaccines (e.g., AV-GBM-1) for glioblastoma, using patient-specific tumor antigens. Comparable therapeutic modality and target indication to Imvax's IGV-001.

TypeBroad incumbent
Description

Owns Keytruda (pembrolizumab), the dominant checkpoint inhibitor, and has historically pursued combination and acquisition strategies in GBM and solid tumor immunotherapy.

TypeBroad incumbent
Description

Major oncology player with broad immunotherapy portfolio and active interest in personalized cell-based approaches for solid tumors. Plausible strategic acquirer of Imvax's autologous platform.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment1 record

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

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds6 records

Each record includes

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

Investors6 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&A

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 →

Imvax

Personalized Cancer Immunotherapyimvax.com

Imvax is a privately held, clinical-stage Philadelphia biotech developing personalized whole-tumor immunotherapies via its proprietary Goldspire® platform, with lead candidate IGV-001 in Phase 2b for newly diagnosed glioblastoma and pipeline programs across multiple solid tumors.

What Imvax does

Imvax is a privately held, clinical-stage biotechnology company founded in 2015 and headquartered in Philadelphia, PA, that develops personalized, whole tumor-derived immunotherapies for solid tumors. The company is built around its proprietary Goldspire® platform, which captures a patient's full tumor antigen signature by combining resected tumor cells with an antisense oligodeoxynucleotide (IMV-001) targeting insulin-like growth factor type 1 receptor (IGF-1R) inside proprietary implantable biodiffusion chambers (BDCs). Tumor samples are processed at Imvax's Philadelphia manufacturing facility in under 24 hours, loaded into BDCs, irradiated, and returned to the hospital for implantation in the patient's abdomen for approximately 48 hours, during which immunogenic cell death releases antigens that stimulate both innate and adaptive immunity.

The lead clinical candidate is IGV-001, an autologous biologic-device combination product for newly diagnosed glioblastoma multiforme (ndGBM), which has received both FDA Fast Track and Orphan Drug Designations. In December 2025, Imvax reported positive Phase 2b top-line data showing median overall survival of 20.3 months versus 14.0 months for placebo (+45% improvement), although the primary progression-free survival endpoint was not met. Approximately 99 patients were enrolled across 19-20 U.S. academic medical centers. The pipeline extends the Goldspire® platform to additional solid tumors, with IHC-001 (hepatocellular carcinoma), IUC-001 (urothelial cancer), IOC-001 (ovarian cancer), and IEC-001 (endometrial cancer) in preclinical or IND-enabling stages.

Imvax has no approved products and no commercial revenue. The company is funded entirely through private capital, having raised approximately $86 million across three rounds between September 2023 and January 2025 from existing and new investors. Distribution of its investigational therapies is exclusively through clinical trial enrollment at major U.S. academic cancer centers. The company is led by Executive Chairman John P. Furey (formerly COO of Spark Therapeutics where he launched LUXTURNA), COO Sean P. Hemingway (formerly Global Head of BioLife Plasma Services at Takeda), and CFO/CLO John M. Limongelli, signaling operational and commercial readiness rather than further research scaling.

Imvax firmographics

Firmographics
Name
Imvax
Legal name
Imvax, Inc.
Website
https://imvax.com
Company type
Private
Founded year
2015
Operating status
Operating
Headcount range
11–50 employees
Short description
Imvax is a privately held, clinical-stage Philadelphia biotech developing personalized whole-tumor immunotherapies via its proprietary Goldspire® platform, with lead candidate IGV-001 in Phase 2b for newly diagnosed glioblastoma and pipeline programs across multiple solid tumors.
Ownership category
akta.pro rank

Imvax industry classification

Industry
Product category
Personalized Cancer Immunotherapy
NAICS
Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Cell Therapy Developers (Autologous) (HLAAABAA)
akta.pro secondary industries
Therapeutic Vaccines (e.g., Cancer/Chronic Infection) (HLAIAEAG), Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies) (HLAAANAK), Therapeutic Vaccines (cancer, chronic infection immunotherapy) (HLAAAEAB)

Keywords

  • Personalized cancer immunotherapy
  • Autologous cell therapy
  • Glioblastoma treatment
  • Tumor-derived vaccines
  • Biologic-device combinations

Where Imvax is headquartered

Location

Headquarters

HQ city
Philadelphia
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Imvax business model

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

Revenue model

  1. Pre-revenue / Clinical Stage Development: Imvax is a clinical-stage biotechnology company with no approved products or commercial revenue. The company is developing personalized immunotherapies for solid tumors, with its lead candidate IGV-001 in Phase 2b clinical development for newly diagnosed glioblastoma. Revenue will depend on successful clinical development, regulatory approval, and commercialization of its pipeline products.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Imvax product offering

Product offering

Core offering

Imvax develops personalized, whole tumor-derived autologous immunotherapies through its proprietary Goldspire® platform. The platform combines patient-derived tumor cells with antisense oligodeoxynucleotide IMV-001 against IGF-1R, loaded into implantable biodiffusion chambers (BDCs), to deliver a full tumor antigen payload and stimulate both innate and adaptive immune responses against residual tumor cells. The lead candidate IGV-001, an autologous biologic-device combination product for newly diagnosed glioblastoma, has reported positive Phase 2b results with median overall survival of 20.3 months versus 14.0 months for placebo.

Product overview

Imvax is a clinical-stage biotechnology company with a platform-plus-products architecture. The core technology is the Goldspire® platform, a personalized, whole tumor-derived immunotherapy that combines patient-derived tumor cells with an antisense oligonucleotide (IMV-001) delivered via proprietary biodiffusion chambers. The lead product is IGV-001 for newly diagnosed glioblastoma, which has completed Phase 2b trials and received FDA Fast Track designation. The pipeline includes multiple programs (IHC-001 for hepatocellular carcinoma, IUC-001 for urothelial cancer, IOC-001 for ovarian cancer, IEC-001 for endometrial cancer, and ICC-001) at various stages from IND-enabling to preclinical studies, all leveraging the same Goldspire® platform technology.

Differentiator

Problem solved

Functional benefit

Brands

  • Goldspire®: Imvax's proprietary immunotherapy platform that delivers personalized, whole tumor-derived immunotherapies by capturing a tumor's full antigen signature and using it to stimulate the patient's innate and adaptive immunity.

Products and services

  • IGV-001 Autologous biologic-device combination product candidate derived from the Goldspire® platform for the treatment of newly diagnosed glioblastoma (ndGBM). Combines patient-derived tumor cells with antisense oligodeoxynucleotide IMV-001 loaded into proprietary biodiffusion chambers implanted for approximately 48 hours. FDA Fast Track Designation and Orphan Drug Designation granted; Phase 2b top-line results announced December 2025 showed median overall survival of 20.3 months versus 14.0 months for placebo (+45%) with no drug-related serious adverse events.
  • IHC-001 Pipeline product candidate for hepatocellular carcinoma (primary liver cancer) being developed using the Goldspire® platform. Preclinical studies are ongoing.
  • IUC-001 Pipeline product candidate for urothelial (bladder) cancer being developed using the Goldspire® platform. Preclinical studies are ongoing.
  • IOC-001 Pipeline product candidate for ovarian cancer being developed using the Goldspire® platform. Preclinical studies are ongoing.
  • IEC-001 Pipeline product candidate for endometrial cancer being developed using the Goldspire® platform. Currently in IND-enabling stage.

Quantifiable outcome

  • Phase 2b trial: Median OS of 20.3 months vs 14.0 months placebo (+45% improvement)
  • +3 more outcomes

Companies that use Imvax

Customer profile

Named customers1 record

Segments1 record

Ideal customer profiles2 records

Imvax technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

Imvax partnerships and signals

Strategic signal

Scale indicators5 records

Recent moves6 records

Expansion highlights5 records

Imvax competitors and assessment

Company assessment

Direct peers

  • Adaptimmune Therapeutics: Develops engineered autologous TCR-T cell therapies for solid tumors. Comparable cell therapy modality and oncology focus to Imvax's Goldspire platform.
  • Iovance Biotherapeutics: Pioneer in tumor-infiltrating lymphocyte (TIL) autologous cell therapy, with an FDA-approved product (Amtagvi) in solid tumors. Comparable as a commercial-stage autologous cell therapy developer in oncology.
  • Mustang Bio: Clinical-stage cell and gene therapy company developing autologous and allogeneic therapies for oncology, including CAR-T programs for solid tumors and hematologic malignancies.
  • Ziopharm Oncology: Develops cell and gene therapies for solid tumors, including autologous CAR-T programs for GBM. Comparable as a clinical-stage personalized cell therapy developer targeting brain tumors.
  • Northwest Biotherapeutics: Developer of DCVax-L, an autologous dendritic cell vaccine for glioblastoma. Closely comparable as both companies pursue personalized cell-based immunotherapy approaches for newly diagnosed GBM.
  • Aivita Biomedical: Develops autologous dendritic cell vaccines (e.g., AV-GBM-1) for glioblastoma, using patient-specific tumor antigens. Comparable therapeutic modality and target indication to Imvax's IGV-001.

Emerging players

  • Candel Therapeutics: Develops viral immunotherapies and autologous cancer vaccines including CAN-3110 for glioblastoma. Adjacent modality but competing in the same indication as Imvax.

Broad incumbents

  • Bristol-Myers Squibb: Large immuno-oncology incumbent with Opdivo (nivolumab) and a broad oncology pipeline. Relevant as a potential strategic acquirer of cell therapy assets like Imvax's IGV-001.
  • Merck & Co. Owns Keytruda (pembrolizumab), the dominant checkpoint inhibitor, and has historically pursued combination and acquisition strategies in GBM and solid tumor immunotherapy.
  • F. Hoffmann-La Roche / Genentech: Major oncology player with broad immunotherapy portfolio and active interest in personalized cell-based approaches for solid tumors. Plausible strategic acquirer of Imvax's autologous platform.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat3 records

Key risks6 records

Key highlights7 records

Customer concentration

Imvax social profiles

Digital presence

Imvax financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Imvax leadership team

Management profile

Number of profiles

Profiles3 records

Imvax funding detail

Funding detail

Funding overview

Funding rounds6 records

Investors6 records

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

Imvax M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Imvax

What does Imvax do?

Imvax develops personalized, whole tumor-derived autologous immunotherapies through its proprietary Goldspire® platform. The platform combines patient-derived tumor cells with antisense oligodeoxynucleotide IMV-001 against IGF-1R, loaded into implantable biodiffusion chambers (BDCs), to deliver a full tumor antigen payload and stimulate both innate and adaptive immune responses against residual tumor cells. The lead candidate IGV-001, an autologous biologic-device combination product for newly diagnosed glioblastoma, has reported positive Phase 2b results with median overall survival of 20.3 months versus 14.0 months for placebo.

Is Imvax a public or private company?

Imvax is a private company. It is classified as venture growth investor backed and is currently operating.

When was Imvax founded?

Imvax was founded in 2015. It employs 11 to 50 people.

Where is Imvax based?

Imvax is headquartered in Philadelphia, United States, in the North America region.

How does Imvax make money?

One revenue line is on record: pre-revenue / Clinical Stage Development.

Who are Imvax's main competitors?

Direct peers on record are Adaptimmune Therapeutics, Iovance Biotherapeutics, Mustang Bio, Ziopharm Oncology, Northwest Biotherapeutics and Aivita Biomedical. Candel Therapeutics is listed as an emerging player. Broad incumbents are Bristol-Myers Squibb, Merck & Co. and F. Hoffmann-La Roche / Genentech.

Does Imvax have an API?

No public API is recorded for Imvax.

What industry is Imvax in?

Imvax's product category is Personalized Cancer Immunotherapy. Its primary akta.pro industry code is HLAAABAA, Cell Therapy Developers (Autologous), with a secondary code of HLAIAEAG, Therapeutic Vaccines (e.g., Cancer/Chronic Infection). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
CuretodayIGV-001 Shows Longer Survival for Newly Diagnosed GlioblastomaPatients with newly diagnosed glioblastoma treated with IGV-001 showed a median overall survival of 20.3 months, surpassing the 14 months seen in the placebo group during a phase 2b clinical trial. The trial results indicate a potential breakthrough for glioblastoma treatment, with no serious side effects reported and plans for further discussions with the FDA regarding regulatory approval. Imvax, the company developing IGV-001, emphasizes the importance of these results in addressing the unmet medical need for this challenging condition.ReviewedNeuro-Oncology Biotech Industry Progress Report 2025The 2025 Brain Tumor Biotech Summit, hosted by Northwell Health Lenox Hill Hospital, the Feinstein Institute for Medical Research, and the Zucker School of Medicine in New York City in June 2025, brought together leaders from academia, biotechnology, and investment to review advances in neuro-oncology including emerging treatments, novel drug delivery platforms, and device-based therapeutics for glioblastoma and other CNS tumors. The summit featured 13 biotech and medtech companies presenting clinical progress reports, with notable developments including Imvax raising $112M in Series C funding, Imaging Biometrics receiving FDA clearance for its MRI-based FTB mapping platform, and early-phase clinical data showing positive signals from therapies including IGV-001, Novocure's TTFields, sonodynamic therapy, and oncomagnetic therapy. The report highlights persistent challenges in neuro-oncology including the blood-brain barrier, tumor heterogeneity, and limited survival improvements beyond the standard 12-14 month prognosis, while emphasizing the growing role of translational partnerships between academia and industry in accelerating therapy development.Venture Capital Access OnlineImvax Inc. Raises $112 Million in Series C FinancingImvax Inc. announced the completion of a $112 million Series C financing led by HP WILD Holding AG with participation from Ziff Capital Partners, Magnetar Capital, TLP Investment Partners, and new investor Invus. The funds will support the Phase 2 clinical development of its lead candidate IGV-001 for glioblastoma multiforme, expand pre-clinical research into other solid tumors, and build operational capabilities. This funding follows promising Phase 1b trial results showing improved survival outcomes compared to standard of care.Clinical Trials ArenaImvax to explore FDA pathway for glioblastoma candidate despite PFS missImvax plans to engage with the US FDA regarding the regulatory pathway for its glioblastoma candidate IGV-001, despite the drug missing its primary endpoint for progression-free survival in a Phase IIb trial. The therapy demonstrated a significant improvement in median overall survival of 20.3 months compared to 14.0 months for the placebo group, while maintaining a consistent safety profile. This development occurs within a competitive landscape where other entities like Kazia Therapeutics and AstraZeneca are also pursuing treatments for this aggressive cancer.FierceBiotechImvax takes brain cancer cell therapy to FDA, betting survival hit will overshadow primary missImvax has submitted a request to the FDA regarding its brain cancer therapy IGV-001, despite failing to meet its primary endpoint in a clinical trial. The trial showed a 6.3-month improvement in median overall survival compared to placebo, a significant finding as the FDA typically prefers overall survival as an endpoint. This development comes amidst a landscape where other drugmakers have struggled to improve existing treatments for glioblastoma.BioSpaceImvax Heads to FDA With 6-Month Survival Gain in Glioblastoma, Despite Endpoint MissPhiladelphia-based biotech Imvax reported that its IGV-001 immunotherapy for newly diagnosed glioblastoma missed the primary endpoint of improving progression-free survival in a Phase IIb trial of 99 patients, though the treatment arm showed a median overall survival of 20.3 months, a six-month improvement over the placebo cohort. The company announced plans to submit a meeting request to the FDA to discuss the regulatory pathway for IGV-001, citing the paucity of treatment options for glioblastoma, which affects approximately 14,000 patients annually in the U.S. IGV-001 is a personalized antisense oligonucleotide immunotherapy derived from Imvax's Goldspire platform, designed to be administered within 24 hours of craniotomy when the blood-brain barrier is temporarily open.Pulse 2.0Imvax: $29 Million Financing Completed To Develop Whole Tumor-Derived ImmunotherapiesImvax closed a $29 million financing round from existing investors to support its Phase 2b trial of IGV-001 in newly diagnosed glioblastoma. The company has raised $86 million in 21 months, and Phase 1 data showed improved median PFS and OS versus historical standard-of-care. The trial's topline results are expected in mid-2025.Business Wire BlogImvax Announces Completion of Enrollment in Phase 2b Clinical Trial of IGV-001 and Successful FinancingImvax, Inc. announced the completion of enrollment in its Phase 2b clinical trial for IGV-001 and received Fast Track designation from the U.S. FDA for treating newly diagnosed glioblastoma. The company also closed a $35 million financing round to support the trial's progression toward top-line data expected by mid-2025.ImvaxImvax Announces Completion of Enrollment in Phase 2b Clinical Trial of IGV-001 and Successful Financing » ImvaxImvax announced the completion of enrollment in its Phase 2b clinical trial for IGV-001, a personalized immunotherapy for newly diagnosed glioblastoma, and secured $35 million in financing. The U.S. Food and Drug Administration (FDA) also granted Fast Track designation to IGV-001 based on existing Phase 1b data. Top-line data from the trial is expected by mid-2025.TechnicalCancer-focused biotech company Imvax raised $23M to advance clinical trialsCancer-focused biotech company Imvax announced the initial closing of a $23 million fundraising round to support its Phase 2b clinical trial for IGV-001, a therapy for glioblastoma. The company also appointed Stephen Webster to its board of directors while David W. Andrews stepped down from the board but remains chief medical officer. Imvax expects the study to be fully enrolled in the first half of 2024.