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Starlight Therapeutics

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uuid000xk9a

Namestring
Starlight Therapeutics
Legal namestring
Starlight Therapeutics Inc.
Company typeenum
Private
Founded yearint
2024
Descriptiontext

Starlight Therapeutics is a clinical-stage precision oncology company focused exclusively on central nervous system (CNS) cancers, operating as a wholly-owned subsidiary of Lantern Pharma Inc. (NASDAQ: LTRN). The company's lead drug candidate, STAR-001 (also known as LP-184), is a tumor-selective prodrug belonging to the acylfulvene class of alkylating antineoplastic agents. STAR-001 exploits synthetic lethality in DNA damage repair (DDR)-deficient tumors by being activated by prostaglandin reductase 1 (PTGR1), an enzyme consistently overexpressed in glioblastomas relative to normal brain tissue. The compound demonstrates nanomolar potency in multiple in vitro and in vivo CNS cancer models, excellent blood-brain barrier permeability comparable to temozolomide, and efficacy irrespective of MGMT promoter methylation status, addressing a major resistance mechanism that limits current standard of care in approximately 65% of glioblastoma cases.

The company's technology platform is anchored by Lantern Pharma's proprietary RADR AI platform, which has analyzed billions of data points to identify patient subgroups and predict therapeutic responses for CNS cancer indications. Drug development is supported by a Scientific Advisory Board comprising internationally recognized neuro-oncology experts from UCSF, Memorial Sloan Kettering Cancer Center, and Johns Hopkins Kimmel Cancer Center. The leadership team includes Founder/Chairman/Acting CEO Panna Sharma, Acting CFO David Margrave, and CMO Marc Chamberlain, who brings extensive academic and industry oncology experience. STAR-001 has secured FDA Orphan Drug Designation, three Rare Pediatric Disease Designations, and Fast-Track Designation for glioblastoma, with FDA IND clearance for a Phase 1 pediatric trial obtained in March 2026.

Starlight Therapeutics is pre-revenue with no commercial product and has no disclosed standalone revenue. Its expected revenue model upon commercialization is prescription drug sales to hospitals, specialty oncology centers, and academic medical centers through specialty pharmacy and formulary channels typical of oncology therapeutics. The company's customer segments target three patient populations: adult glioblastoma patients (approximately 13,000 annual US cases), brain metastases patients from lung, breast, and melanoma primaries (100,000+ annual US cases), and pediatric CNS cancer patients including ultra-rare ATRT and DIPG (4,000+ annual US cases). The aggregate annual US market potential is estimated at $5-6 billion, with the company explicitly pursuing indications lacking accepted standard of care. As of April 2026, the company has 1-10 employees and operates from Plano, Texas, with clinical trial sites planned across the US, Canada, and Israel through the POETIC consortium.

Short descriptiontext

Starlight Therapeutics, a wholly-owned subsidiary of Lantern Pharma, is a clinical-stage precision oncology company developing STAR-001, a synthetic lethality prodrug for adult and pediatric CNS cancers including glioblastoma, brain metastases, and ultra-rare pediatric tumors. The company leverages AI for development.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersPlano, United States
HQ citystring
Plano
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
precision oncology therapeutics, CNS cancer treatment, glioblastoma drug development, brain cancer therapy, AI-driven drug discovery
Industry2 codes
1Neuro-Oncology
CodeHLAKAFAHPrimaryYes
2Drug Discovery (Target ID/Validation & Hit Discovery)
CodeHLAIALAAPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Precision Oncology Therapeutics
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Drug Sales
TypeOne Time License
Description

Starlight is a pre-revenue clinical-stage precision oncology company. Its primary expected revenue stream will come from the commercialization of STAR-001 and potentially other pipeline candidates upon successful clinical development and FDA approval. Revenue would be generated through prescription drug sales in the US and potentially international markets.

starlightthera.com
Marketing channels6 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, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Starlight Therapeutics is developing STAR-001 (LP-184), a brain-permeable, tumor-site-activated acylfulvene prodrug that leverages synthetic lethality in DNA damage repair (DDR)-deficient tumors. STAR-001 is activated by prostaglandin reductase 1 (PTGR1), which is overexpressed in CNS tumors, enabling selective cytotoxicity across glioblastoma, brain metastases, and rare pediatric CNS cancers including ATRT and DIPG. The company is advancing the asset through multi-phase clinical trials at leading academic medical centers toward FDA approval.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • In preclinical ATRT models, STAR-001 and spironolactone combination extended median survival by 181% compared to control.
+3 more records
Product overview1 text field

Starlight Therapeutics is a precision oncology company focused solely on CNS (central nervous system) cancers, primarily brain cancers. The company is developing STAR-001 as its lead drug candidate for multiple CNS malignancies including glioblastoma, brain metastases, and rare pediatric CNS cancers. STAR-001 is supported by AI platforms including RADR for predictive analytics and patient stratification, and withZeta.ai for multi-agentic drug discovery assistance. The company operates as a wholly-owned subsidiary of Lantern Pharma (NASDAQ: LTRN) with operations in Plano, Texas.

Product and service2 records
1STAR-001 (LP-184)
CategoryOncology Drug Candidate
Description

STAR-001 (LP-184) is a highly potent, brain-permeable small-molecule prodrug belonging to the acylfulvene class of alkylating antineoplastic agents. It targets both adult and pediatric CNS tumors through synthetic lethality, exploiting DNA damage repair vulnerabilities in tumor cells while sparing healthy cells, and is activated by PTGR1 which is overexpressed in glioblastomas. STAR-001 is being advanced through multi-phase clinical trials for glioblastoma, brain metastases, and rare pediatric CNS cancers.

2withZeta.ai
CategoryAI Drug Discovery Platform
Description

withZeta.ai is a multi-agentic AI co-scientist platform designed to accelerate rare and complex cancer drug development by integrating multiple AI modalities through autonomous agent workflows. It supports precision oncology development for CNS cancers and other rare tumor types.

Scale indicator12 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
1POETIC (Pediatric Oncology Experimental Therapeutics Investigators' Consortium)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Starlight Therapeutics collaborates with POETIC for the conduct of its planned Phase I pediatric CNS cancer trial of STAR-001. The trial will enroll 18 to 42 patients aged 1-17 with relapsed or refractory CNS malignancies including DIPG, ATRT, medulloblastoma, ependymoma, and glioblastoma at approximately 15 leading academic pediatric oncology centers in the US, Canada, and Israel.

clinicaltrialsarena.com
Strategic tierCoreTypeOthers
Description

Starlight Therapeutics is a wholly owned subsidiary of Lantern Pharma (NASDAQ: LTRN). Lantern provides the RADR AI platform powering STAR-001's development, shared infrastructure, and clinical operations. The formation of Starlight allows Lantern to dedicate focused resources to advancing STAR-001 through targeted clinical trials.

3World-Leading Cancer Researchers
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Starlight was 'born from billions of data points using AI and in collaboration with world-class cancer researchers.' The company has established a Scientific Advisory Board with internationally recognized neuro-oncology experts from UCSF, Memorial Sloan Kettering Cancer Center, and Johns Hopkins Kimmel Cancer Center who provide strategic guidance on clinical development and scientific strategy.

starlightthera.com
Recent move11 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Oncology company developing antibody-drug conjugates with precision targeting approaches. Comparable in precision oncology drug development methodology, though at a more advanced commercial stage.

TypeDirect peer
Description

Clinical-stage oncology company focused on brain cancer, including lead asset paxalisib for glioblastoma. Directly comparable as a small-cap CNS oncology biotech pursuing regulatory designations in GBM.

TypeDirect peer
Description

Clinical-stage oncology company developing therapies that target the tumor microenvironment, with applications in CNS cancers. Comparable in clinical-stage profile and oncology focus including GBM.

TypeDirect peer
Description

Clinical-stage oncology company developing targeted radiotherapeutics for CNS cancers, including glioblastoma. Comparable in clinical stage, indication focus, and small-cap biotech profile.

TypeDirect peer
Description

Clinical-stage CNS-focused biopharmaceutical company developing therapeutics for seizure disorders and rare neurological diseases. Comparable as a CNS-focused biotech with FDA-designated programs.

TypeBroad incumbent
Description

Parent company and developer of the RADR AI platform used by Starlight. Lantern is a publicly-traded AI-driven precision oncology company with a broader pipeline beyond CNS; directly comparable as the originator and sponsor of STAR-001/LP-184.

TypeEmerging player
Description

Clinical-stage precision oncology company developing targeted therapies exploiting DNA damage response pathways. Comparable in synthetic lethality / DDR-targeting approach and clinical-stage biotech profile.

TypeDirect peer
Description

Clinical-stage oncology company focused on CNS cancers including glioblastoma with lead asset VAL-083. Comparable as a small-cap CNS oncology biotech pursuing FDA-designated GBM therapy.

TypeBroad incumbent
Description

Clinical-stage biopharmaceutical company developing oncology therapeutics. Comparable in clinical-stage biopharma structure and oncology drug development, though with broader indication scope than Starlight.

TypeDirect peer
Description

Clinical-stage company developing Berubicin for glioblastoma and other CNS tumors. Highly comparable as a CNS-oncology-focused small biotech with similar regulatory strategy and clinical-stage asset profile.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 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 highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

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

Ideal customer profile1 record

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 capability5 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

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

Investors

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 →

Starlight Therapeutics

Precision Oncology Therapeuticsstarlightthera.com

Starlight Therapeutics, a wholly-owned subsidiary of Lantern Pharma, is a clinical-stage precision oncology company developing STAR-001, a synthetic lethality prodrug for adult and pediatric CNS cancers including glioblastoma, brain metastases, and ultra-rare pediatric tumors. The company leverages AI for development.

What Starlight Therapeutics does

Starlight Therapeutics is a clinical-stage precision oncology company focused exclusively on central nervous system (CNS) cancers, operating as a wholly-owned subsidiary of Lantern Pharma Inc. (NASDAQ: LTRN). The company's lead drug candidate, STAR-001 (also known as LP-184), is a tumor-selective prodrug belonging to the acylfulvene class of alkylating antineoplastic agents. STAR-001 exploits synthetic lethality in DNA damage repair (DDR)-deficient tumors by being activated by prostaglandin reductase 1 (PTGR1), an enzyme consistently overexpressed in glioblastomas relative to normal brain tissue. The compound demonstrates nanomolar potency in multiple in vitro and in vivo CNS cancer models, excellent blood-brain barrier permeability comparable to temozolomide, and efficacy irrespective of MGMT promoter methylation status, addressing a major resistance mechanism that limits current standard of care in approximately 65% of glioblastoma cases.

The company's technology platform is anchored by Lantern Pharma's proprietary RADR AI platform, which has analyzed billions of data points to identify patient subgroups and predict therapeutic responses for CNS cancer indications. Drug development is supported by a Scientific Advisory Board comprising internationally recognized neuro-oncology experts from UCSF, Memorial Sloan Kettering Cancer Center, and Johns Hopkins Kimmel Cancer Center. The leadership team includes Founder/Chairman/Acting CEO Panna Sharma, Acting CFO David Margrave, and CMO Marc Chamberlain, who brings extensive academic and industry oncology experience. STAR-001 has secured FDA Orphan Drug Designation, three Rare Pediatric Disease Designations, and Fast-Track Designation for glioblastoma, with FDA IND clearance for a Phase 1 pediatric trial obtained in March 2026.

Starlight Therapeutics is pre-revenue with no commercial product and has no disclosed standalone revenue. Its expected revenue model upon commercialization is prescription drug sales to hospitals, specialty oncology centers, and academic medical centers through specialty pharmacy and formulary channels typical of oncology therapeutics. The company's customer segments target three patient populations: adult glioblastoma patients (approximately 13,000 annual US cases), brain metastases patients from lung, breast, and melanoma primaries (100,000+ annual US cases), and pediatric CNS cancer patients including ultra-rare ATRT and DIPG (4,000+ annual US cases). The aggregate annual US market potential is estimated at $5-6 billion, with the company explicitly pursuing indications lacking accepted standard of care. As of April 2026, the company has 1-10 employees and operates from Plano, Texas, with clinical trial sites planned across the US, Canada, and Israel through the POETIC consortium.

Starlight Therapeutics firmographics

Firmographics
Name
Starlight Therapeutics
Legal name
Starlight Therapeutics Inc.
Website
https://starlightthera.com
Company type
Private
Founded year
2024
Operating status
Operating
Headcount range
1–10 employees
Short description
Starlight Therapeutics, a wholly-owned subsidiary of Lantern Pharma, is a clinical-stage precision oncology company developing STAR-001, a synthetic lethality prodrug for adult and pediatric CNS cancers including glioblastoma, brain metastases, and ultra-rare pediatric tumors. The company leverages AI for development.
Ownership category
akta.pro rank

Starlight Therapeutics industry classification

Industry
Product category
Precision Oncology Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Neuro-Oncology (HLAKAFAH)
akta.pro secondary industry
Drug Discovery (Target ID/Validation & Hit Discovery) (HLAIALAA)

Keywords

  • Precision oncology therapeutics
  • CNS cancer treatment
  • Glioblastoma drug development
  • Brain cancer therapy
  • AI-driven drug discovery

Where Starlight Therapeutics is headquartered

Location

Headquarters

HQ city
Plano
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Starlight Therapeutics business model

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

Revenue model

  1. Pharmaceutical Drug Sales: Starlight is a pre-revenue clinical-stage precision oncology company. Its primary expected revenue stream will come from the commercialization of STAR-001 and potentially other pipeline candidates upon successful clinical development and FDA approval. Revenue would be generated through prescription drug sales in the US and potentially international markets.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels6 records

Starlight Therapeutics product offering

Product offering

Core offering

Starlight Therapeutics is developing STAR-001 (LP-184), a brain-permeable, tumor-site-activated acylfulvene prodrug that leverages synthetic lethality in DNA damage repair (DDR)-deficient tumors. STAR-001 is activated by prostaglandin reductase 1 (PTGR1), which is overexpressed in CNS tumors, enabling selective cytotoxicity across glioblastoma, brain metastases, and rare pediatric CNS cancers including ATRT and DIPG. The company is advancing the asset through multi-phase clinical trials at leading academic medical centers toward FDA approval.

Product overview

Starlight Therapeutics is a precision oncology company focused solely on CNS (central nervous system) cancers, primarily brain cancers. The company is developing STAR-001 as its lead drug candidate for multiple CNS malignancies including glioblastoma, brain metastases, and rare pediatric CNS cancers. STAR-001 is supported by AI platforms including RADR for predictive analytics and patient stratification, and withZeta.ai for multi-agentic drug discovery assistance. The company operates as a wholly-owned subsidiary of Lantern Pharma (NASDAQ: LTRN) with operations in Plano, Texas.

Differentiator

Problem solved

Functional benefit

Products and services

  • STAR-001 (LP-184) STAR-001 (LP-184) is a highly potent, brain-permeable small-molecule prodrug belonging to the acylfulvene class of alkylating antineoplastic agents. It targets both adult and pediatric CNS tumors through synthetic lethality, exploiting DNA damage repair vulnerabilities in tumor cells while sparing healthy cells, and is activated by PTGR1 which is overexpressed in glioblastomas. STAR-001 is being advanced through multi-phase clinical trials for glioblastoma, brain metastases, and rare pediatric CNS cancers.
  • withZeta.ai withZeta.ai is a multi-agentic AI co-scientist platform designed to accelerate rare and complex cancer drug development by integrating multiple AI modalities through autonomous agent workflows. It supports precision oncology development for CNS cancers and other rare tumor types.

Quantifiable outcome

  • In preclinical ATRT models, STAR-001 and spironolactone combination extended median survival by 181% compared to control.
  • +3 more outcomes

Companies that use Starlight Therapeutics

Customer profile

Segments3 records

Ideal customer profiles1 record

Starlight Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability5 records

Feature5 records

Starlight Therapeutics partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core.

  • POETIC (Pediatric Oncology Experimental Therapeutics Investigators' Consortium)coreStrategic or Co-development PartnerStarlight Therapeutics collaborates with POETIC for the conduct of its planned Phase I pediatric CNS cancer trial of STAR-001. The trial will enroll 18 to 42 patients aged 1-17 with relapsed or refractory CNS malignancies including DIPG, ATRT, medulloblastoma, ependymoma, and glioblastoma at approximately 15 leading academic pediatric oncology centers in the US, Canada, and Israel.
  • Lantern Pharma (Parent Company)coreOthersStarlight Therapeutics is a wholly owned subsidiary of Lantern Pharma (NASDAQ: LTRN). Lantern provides the RADR AI platform powering STAR-001's development, shared infrastructure, and clinical operations. The formation of Starlight allows Lantern to dedicate focused resources to advancing STAR-001 through targeted clinical trials.
  • World-Leading Cancer ResearcherscoreStrategic or Co-development PartnerStarlight was 'born from billions of data points using AI and in collaboration with world-class cancer researchers.' The company has established a Scientific Advisory Board with internationally recognized neuro-oncology experts from UCSF, Memorial Sloan Kettering Cancer Center, and Johns Hopkins Kimmel Cancer Center who provide strategic guidance on clinical development and scientific strategy.

Scale indicators12 records

Recent moves11 records

Expansion highlights5 records

Starlight Therapeutics competitors and assessment

Company assessment

Broad incumbents

  • ImmunoGen: Oncology company developing antibody-drug conjugates with precision targeting approaches. Comparable in precision oncology drug development methodology, though at a more advanced commercial stage.
  • Lantern Pharma: Parent company and developer of the RADR AI platform used by Starlight. Lantern is a publicly-traded AI-driven precision oncology company with a broader pipeline beyond CNS; directly comparable as the originator and sponsor of STAR-001/LP-184.
  • Chimerix: Clinical-stage biopharmaceutical company developing oncology therapeutics. Comparable in clinical-stage biopharma structure and oncology drug development, though with broader indication scope than Starlight.

Direct peers

  • Kazia Therapeutics: Clinical-stage oncology company focused on brain cancer, including lead asset paxalisib for glioblastoma. Directly comparable as a small-cap CNS oncology biotech pursuing regulatory designations in GBM.
  • Diffusion Pharmaceuticals: Clinical-stage oncology company developing therapies that target the tumor microenvironment, with applications in CNS cancers. Comparable in clinical-stage profile and oncology focus including GBM.
  • PLUS Therapeutics: Clinical-stage oncology company developing targeted radiotherapeutics for CNS cancers, including glioblastoma. Comparable in clinical stage, indication focus, and small-cap biotech profile.
  • Marinus Pharmaceuticals: Clinical-stage CNS-focused biopharmaceutical company developing therapeutics for seizure disorders and rare neurological diseases. Comparable as a CNS-focused biotech with FDA-designated programs.
  • Kintara Therapeutics: Clinical-stage oncology company focused on CNS cancers including glioblastoma with lead asset VAL-083. Comparable as a small-cap CNS oncology biotech pursuing FDA-designated GBM therapy.
  • CNS Pharmaceuticals: Clinical-stage company developing Berubicin for glioblastoma and other CNS tumors. Highly comparable as a CNS-oncology-focused small biotech with similar regulatory strategy and clinical-stage asset profile.

Emerging players

  • Aprea Therapeutics: Clinical-stage precision oncology company developing targeted therapies exploiting DNA damage response pathways. Comparable in synthetic lethality / DDR-targeting approach and clinical-stage biotech profile.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Starlight Therapeutics social profiles

Digital presence

Starlight Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Starlight Therapeutics leadership team

Management profile

Number of profiles

Profiles3 records

Starlight Therapeutics funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors

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

Starlight Therapeutics 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 Starlight Therapeutics

What does Starlight Therapeutics do?

Starlight Therapeutics is developing STAR-001 (LP-184), a brain-permeable, tumor-site-activated acylfulvene prodrug that leverages synthetic lethality in DNA damage repair (DDR)-deficient tumors. STAR-001 is activated by prostaglandin reductase 1 (PTGR1), which is overexpressed in CNS tumors, enabling selective cytotoxicity across glioblastoma, brain metastases, and rare pediatric CNS cancers including ATRT and DIPG. The company is advancing the asset through multi-phase clinical trials at leading academic medical centers toward FDA approval.

Is Starlight Therapeutics a public or private company?

Starlight Therapeutics is a private company. It is classified as corporate owned and is currently operating.

When was Starlight Therapeutics founded?

Starlight Therapeutics was founded in 2024. It employs 1 to 10 people.

Where is Starlight Therapeutics based?

Starlight Therapeutics is headquartered in Plano, United States, in the North America region.

How does Starlight Therapeutics make money?

One revenue line is on record: pharmaceutical Drug Sales.

Who are Starlight Therapeutics's main competitors?

Broad incumbents on record are ImmunoGen, Lantern Pharma and Chimerix. Direct peers are Kazia Therapeutics, Diffusion Pharmaceuticals, PLUS Therapeutics, Marinus Pharmaceuticals, Kintara Therapeutics and CNS Pharmaceuticals. Aprea Therapeutics is listed as an emerging player.

Does Starlight Therapeutics have an API?

No public API is recorded for Starlight Therapeutics.

What industry is Starlight Therapeutics in?

Starlight Therapeutics's product category is Precision Oncology Therapeutics. Its primary akta.pro industry code is HLAKAFAH, Neuro-Oncology, with a secondary code of HLAIALAA, Drug Discovery (Target ID/Validation & Hit Discovery). Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
BioSpaceLantern Pharma Reports First Quarter 2026 Financial Results and Provides Business UpdatesLantern Pharma reported Q1 2026 results with a 27% year-over-year net loss reduction and a 47% R&D spend cut. The company launched withZeta.ai, a multi-agentic AI platform, and received FDA clearance for a pediatric CNS cancer trial. It plans to separate withZeta.ai into an independent entity and expects operations to fund into Q1 2027.openPR.comGlioblastoma Multiforme Market: Rapid Growth & Investment Outlook to 2034 - DelveInsightDelveInsight's market report on Glioblastoma Multiforme (GBM) estimates the market was valued at approximately USD 835 million in 2023 and is expected to grow significantly through 2034, driven by increasing disease prevalence and a robust pipeline of therapeutic candidates. Key recent developments include FDA orphan drug designation for Exousia Pro's exosome-based therapy (October 2025), Starlight Therapeutics' FDA IND approval for a Phase Ib/2a trial combining STAR-001 with spironolactone (August 2025), Diakonos Oncology's $20 million funding round to advance its Phase II GBM trial of dubodencel (June 2025), and Novocure's FDA approval of new HFE transducer arrays for OPTUNE GIO (November 2024).European BiotechnologyEurope’s distinct biotech venture studio modelEuropean biotech venture studios are emerging as a minority formation model, with AQYLA BioVentures and 4P-Pharma exemplifying internal target origination and risk compartmentalization. AQYLA's first programme, STARLIGHT Therapeutics, secured €1.8mn in seed funding, while 4P-Pharma uses a hybrid structure to isolate program-specific risks. The European model is expected to evolve with its own strengths, distinct from the U.S. hub-and-spoke system.Clinical Trials ArenaLantern receives FDA clearance for paediatric STAR-001 CNS trialLantern Pharma, a subsidiary of Starlight Therapeutics, has received FDA clearance for its investigational new drug application to initiate a Phase I pediatric CNS cancer trial of STAR-001 in combination with spironolactone at approximately 15 centers in Canada, Israel, and the US. The dose-escalation, open-label trial will enroll 18 to 42 patients aged one to 17 years with relapsed or refractory CNS malignancies, including DIPG, ATRT, medulloblastoma, ependymoma, and glioblastoma, through the POETIC research network. In preclinical ATRT models, the STAR-001 and spironolactone combination extended median survival by 181% compared to control, though additional funding is required before trial commencement.Business Wire BlogLantern Pharma and Starlight Therapeutics Announce FDA Clearance of IND for a Planned Phase 1 Pediatric CNS Cancer Trial of STAR-001The FDA has cleared Lantern Pharma and Starlight Therapeutics' Investigational New Drug (IND) application to proceed with a planned Phase 1 pediatric clinical trial of STAR-001 (LP-184) for children with relapsed or refractory CNS malignancies including ATRT, DIPG, GBM, medulloblastoma, and ependymoma. The multicenter trial will evaluate STAR-001 as monotherapy and in combination with spironolactone across approximately 15 leading academic pediatric oncology centers in collaboration with POETIC, spanning the United States, Canada, and Israel. In preclinical ATRT models, the combination extended median survival by 181% compared to control, and the trial is designed to enroll 18 to 42 patients aged 1 to 17 years, subject to obtaining additional funding.BioSpaceLantern Pharma and Starlight Therapeutics Announce FDA Clearance of IND for a Planned Phase 1 Pediatric CNS Cancer Trial of STAR-001Lantern Pharma and its wholly owned subsidiary Starlight Therapeutics announced FDA clearance of their Investigational New Drug application for STAR-001, a precision oncology compound, to begin a planned Phase 1 pediatric clinical trial for children with relapsed or refractory CNS malignancies including ATRT, DIPG, GBM, medulloblastoma, and ependymoma. The multicenter trial will evaluate STAR-001 as monotherapy and in combination with spironolactone in approximately 18 to 42 patients aged 1 to 17 across 15 leading academic pediatric oncology centers spanning the United States, Canada, and Israel. Preclinical data showed the combination extended median survival by 181% in ATRT models compared to control, with the trial to be conducted in collaboration with POETIC (Pediatric Oncology Experimental Therapeutics Investigators' Consortium).Business Wire BlogLantern Pharma Reports Third Quarter 2025 Financial Results and Provides Business UpdatesLantern Pharma reported a transformational Q3 2025 with its LP-184 Phase 1a trial achieving all primary endpoints, demonstrating a 48% clinical benefit rate in evaluable cancer patients at therapeutic dose threshold with marked tumor reductions in patients with DNA damage repair mutations including CHK2, ATM, and STK11/KEAP1 alterations. The company completed a productive FDA Type C meeting providing regulatory pathway clarity for subsidiary Starlight Therapeutics' planned pediatric CNS cancer trial in Atypical Teratoid Rhabdoid Tumor, with cash position of approximately $12.4 million providing runway into Q3 2026.