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Quince Therapeutics

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uuid0000fcx

Namestring
Quince Therapeutics
Legal namestring
Quince Therapeutics, Inc.
Websiteurl
quincetx.com
Company typeenum
Public
Founded yearint
2022
Descriptiontext

Quince Therapeutics, Inc. is a South San Francisco-based, NASDAQ-listed (QNCX) late-stage biotechnology company developing therapeutics for rare diseases using its proprietary Autologous Intracellular Drug Encapsulation (AIDE) platform. The AIDE technology is an automated drug/device combination that encapsulates drugs into a patient's own red blood cells using a CE-marked RCL (Red Cell Loader) automated point-of-care device paired with a CE-marked single-use sterile treatment kit (EryKit), designed to improve biodistribution, prolong circulating half-life, and reduce immunogenicity for small molecules, large molecules, peptides, proteins, and biologics.

The lead clinical asset, eDSP (encapsulated dexamethasone sodium phosphate, formerly EryDex), applied the AIDE platform to corticosteroid delivery and was developed primarily for Ataxia-Telangiectasia and Duchenne Muscular Dystrophy, with a publicly disclosed list of eleven additional rare disease indications being pursued via licensing. The pivotal Phase 3 NEAT trial of eDSP in Ataxia-Telangiectasia failed its primary endpoint in January 2026, prompting a strategic alternatives process and severe financial distress. In May 2026, Quince acquired Orphai Therapeutics and added LAM-001, an inhaled rapamycin product with U.S. and EU orphan drug designations targeting Pulmonary Arterial Hypertension and Pulmonary Hypertension associated with Interstitial Lung Disease, currently in Phase 2.

Quince generates no current revenue and operates a pre-commercial licensing-and-partnership revenue model: business development outreach ([email protected]) is the primary commercial channel, supplemented by an enterprise advisor-led motion via LifeSci Capital. The company has grown primarily through acquisitions (Novosteo 2022, EryDel 2023, Orphai 2026) and has been funded through a combination of post-IPO equity and pre-IPO venture rounds totaling over $360 million historically, with an up to $187 million private placement announced alongside the Orphai deal to fund the integrated pulmonary pipeline.

Short descriptiontext

Quince Therapeutics is a NASDAQ-listed, late-stage rare disease biotech developing drug/device therapies based on its proprietary AIDE red blood cell encapsulation platform, with a lead Phase 3-failed asset (eDSP) and a newly acquired inhaled rapamycin program (LAM-001) for pulmonary disorders.

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

Serves global market

Keyword5 values
rare disease therapeutics, drug delivery platform, red blood cell encapsulation, autologous drug device combination, clinical stage biotechnology
Industry1 code
1CRISPR & Functional Genomics Screening Platforms (pooled/arrayed screens, perturb-seq)
CodeHLAAAIAGPrimaryYes
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Medicinal and Botanical Manufacturing325411
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Services-Commercial Physical & Biological Research8731
Product category
Rare Disease Biopharmaceuticals
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1No current revenue
TypeSubscription Recurring
Description

Quince Therapeutics reports no revenue. The company is pre-commercial, with a negative EPS of -10.62 (as of May 2026) and product candidates still in clinical development or recently failed trials.

gurufocus.com
2Future licensing royalties (planned)
TypeLicensing Royalties
Description

The Pipeline page invites inbound licensing inquiries via [email protected] for eDSP across additional indications (DMD and prioritized rare disease targets such as autoimmune hepatitis, pulmonary sarcoidosis, dermatomyositis, pemphigus vulgaris, Hashimoto's encephalopathy, Becker muscular dystrophy, pediatric lupus, juvenile idiopathic arthritis, myasthenia gravis, limb-girdle muscular dystrophy, and chronic inflammatory demyelinating polyradiculoneuropathy). Implies a future licensing/royalty revenue model contingent on regulatory approval.

quincetx.com
Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1AIDE (Autologous Intracellular Drug Encapsulation)
Description

Proprietary drug/device combination technology platform that encapsulates drugs into a patient's own red blood cells using the RCL device and single-use treatment kit.

quincetx.com
+1 more record
Core offering1 text field

Quince Therapeutics is a late-stage, pre-commercial biotechnology company developing drug/device combination therapeutics for rare diseases using its proprietary AIDE (Autologous Intracellular Drug Encapsulation) platform. The AIDE platform pairs the CE-marked RCL (Red Cell Loader) automated device with a CE-marked sterile single-use treatment kit to encapsulate drugs inside a patient's own red blood cells at the point of care in approximately two hours. Its lead clinical-stage product eDSP (encapsulated dexamethasone sodium phosphate) is being developed for Ataxia-Telangiectasia and Duchenne Muscular Dystrophy, and the company added the inhaled rapamycin product LAM-001 for rare pulmonary disorders via its May 2026 acquisition of Orphai Therapeutics.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Quince Therapeutics operates a single integrated product architecture centered on its proprietary AIDE (Autologous Intracellular Drug Encapsulation) technology platform, which pairs the CE-marked RCL (Red Cell Loader) automated device with a CE-marked single-use treatment kit to encapsulate drugs into a patient's own red blood cells at the point of care. The lead clinical-stage product eDSP (encapsulated dexamethasone sodium phosphate, formerly EryDex, acquired via the 2023 EryDel acquisition) is the first drug to leverage this platform, with clinical programs in Ataxia-Telangiectasia (lead indication, Phase 3 NEAT failed in February 2026) and Duchenne Muscular Dystrophy (second indication, Phase 2 study designs finalized). The platform architecture and underlying RCL/EryKit consumables support broader indication expansion (autoimmune hepatitis, pulmonary sarcoidosis, dermatomyositis, pemphigus vulgaris, Hashimoto's encephalopathy, Becker muscular dystrophy, pediatric lupus, juvenile idiopathic arthritis, myasthenia gravis, limb-girdle muscular dystrophy, and chronic inflammatory demyelinating polyradiculoneuropathy). In May 2026 Quince expanded its portfolio through the acquisition of Orphai Therapeutics, adding the inhaled rapamycin product LAM-001 for rare pulmonary disorders (PAH and PH-ILD). The 2022 Novosteo acquisition and corporate rebrand from Cortexyme to Quince Therapeutics completed the pipeline focus on rare-disease therapeutics.

Product and service5 records
1AIDE Technology Platform (Autologous Intracellular Drug Encapsulation)
CategoryCore technology platform / drug delivery
Description

Proprietary drug/device combination platform that uses an automated process to encapsulate a drug into a patient's own red blood cells, designed to harness benefits including potentially better tolerability, enhanced tissue biodistribution, reduced immunogenicity, and prolongation of circulating half-life; applicable to small molecules, large molecules, peptides, proteins, and biologics.

2eDSP (encapsulated Dexamethasone Sodium Phosphate; previously EryDex)
CategoryClinical-stage drug product (rare disease therapeutics)
Description

First product leveraging the AIDE technology platform, composed of dexamethasone sodium phosphate (DSP) encapsulated in autologous red blood cells; designed to maintain corticosteroid efficacy while reducing or eliminating chronic toxicity such as adrenal suppression, with lead development in Ataxia-Telangiectasia and Duchenne Muscular Dystrophy.

3RCL (Red Cell Loader) Device
CategoryProprietary medical device
Description

Proprietary CE-marked non-invasive automated device that performs blood processing at the point of care to automate the AIDE encapsulation process; features a touchscreen interface with three microprocessor circuit boards and handles blood, drug, and processing solutions using the single-use treatment kit.

4Single-Use Treatment Kit (EryKit consumables)
CategoryMedical device consumables
Description

CE-marked sterile, single-use, pyrogen-free disposable blood tubing system used with the RCL to encapsulate small molecules, large molecules, and biologics into human red blood cells; contains a centrifuge, hemoconcentrator filter, bags, organizer cassette, and accessories.

5LAM-001 (inhaled formulation of rapamycin)
CategoryClinical-stage drug product (rare pulmonary disease therapeutics)
Description

Inhaled formulation of rapamycin targeting rare pulmonary disorders including Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension associated with Interstitial Lung Disease (PH-ILD); holds U.S. and EU orphan drug designations across multiple indications.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Commercial-stage company with YUTREPIA, an inhaled treprostinil for PAH/PH-ILD, putting it in direct therapeutic-area competition with Quince's LAM-001 program.

TypeBroad incumbent
Description

Established rare-disease biotech with multiple approved products and a broad rare-disease pipeline; a natural strategic acquirer/partner comparable for Quince given its rare-disease focus and clinical-stage assets.

TypeBroad incumbent
Description

Commercial leader in PAH (Tyvaso, Remodulin, Orenitram) and a key competitor for any inhaled pulmonary asset; relevant comparator for LAM-001's commercial potential in PAH and PH-ILD.

TypeBroad incumbent
Description

Major rare-disease commercial player (Naglazyme, Vimizim, Voxzogo, Roctavian) with a long history of orphan drug development and acquisitions of late-stage rare-disease assets — relevant benchmark and potential acquirer profile.

TypeDirect peer
Description

French biotech that develops red blood cell-encapsulated therapeutics (eryaspase, Graspa) — historically the closest direct peer to Quince's AIDE red-cell encapsulation platform, focused on rare metabolic and oncology indications.

TypeBroad incumbent
Description

Established rare-disease franchise within AstraZeneca (Soliris, Ultomiris, Strensiq); a benchmark for rare-disease commercial execution and a potential acquirer/partner for AIDE-derived programs.

TypeEmerging player
Description

Clinical-stage biotech focused on rare muscle disorders including Duchenne and Becker muscular dystrophy — directly comparable for Quince's eDSP DMD/Becker MD programs.

TypeDirect peer
Description

Late-stage clinical biotech developing seralutinib for PAH; a direct competitor in the rare pulmonary hypertension space where LAM-001 is being positioned.

TypeBroad incumbent
Description

Specialty rare-disease biopharma with a portfolio that includes corticosteroids and inflammatory/immunology indications overlapping with the eDSP pipeline expansion list (DMD, JIA, autoimmune diseases).

TypeEmerging player
Description

Rare pulmonary-disease biotech (approved ARIKAYCE for MAC lung disease and a Phase 3 program in PH-ILD); comparable business model and therapeutic focus to LAM-001's PAH/PH-ILD positioning.

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

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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

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

Subsidiaries3 records

Each record includes

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

Compliance4 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds8 records

Each record includes

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

Investors30 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&A3 records

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 →

Quince Therapeutics

Rare Disease Biopharmaceuticalsquincetx.com

Quince Therapeutics is a NASDAQ-listed, late-stage rare disease biotech developing drug/device therapies based on its proprietary AIDE red blood cell encapsulation platform, with a lead Phase 3-failed asset (eDSP) and a newly acquired inhaled rapamycin program (LAM-001) for pulmonary disorders.

What Quince Therapeutics does

Quince Therapeutics, Inc. is a South San Francisco-based, NASDAQ-listed (QNCX) late-stage biotechnology company developing therapeutics for rare diseases using its proprietary Autologous Intracellular Drug Encapsulation (AIDE) platform. The AIDE technology is an automated drug/device combination that encapsulates drugs into a patient's own red blood cells using a CE-marked RCL (Red Cell Loader) automated point-of-care device paired with a CE-marked single-use sterile treatment kit (EryKit), designed to improve biodistribution, prolong circulating half-life, and reduce immunogenicity for small molecules, large molecules, peptides, proteins, and biologics.

The lead clinical asset, eDSP (encapsulated dexamethasone sodium phosphate, formerly EryDex), applied the AIDE platform to corticosteroid delivery and was developed primarily for Ataxia-Telangiectasia and Duchenne Muscular Dystrophy, with a publicly disclosed list of eleven additional rare disease indications being pursued via licensing. The pivotal Phase 3 NEAT trial of eDSP in Ataxia-Telangiectasia failed its primary endpoint in January 2026, prompting a strategic alternatives process and severe financial distress. In May 2026, Quince acquired Orphai Therapeutics and added LAM-001, an inhaled rapamycin product with U.S. and EU orphan drug designations targeting Pulmonary Arterial Hypertension and Pulmonary Hypertension associated with Interstitial Lung Disease, currently in Phase 2.

Quince generates no current revenue and operates a pre-commercial licensing-and-partnership revenue model: business development outreach ([email protected]) is the primary commercial channel, supplemented by an enterprise advisor-led motion via LifeSci Capital. The company has grown primarily through acquisitions (Novosteo 2022, EryDel 2023, Orphai 2026) and has been funded through a combination of post-IPO equity and pre-IPO venture rounds totaling over $360 million historically, with an up to $187 million private placement announced alongside the Orphai deal to fund the integrated pulmonary pipeline.

Quince Therapeutics firmographics

Firmographics
Name
Quince Therapeutics
Legal name
Quince Therapeutics, Inc.
Website
https://quincetx.com
Company type
Public
Founded year
2022
Operating status
Operating
Headcount range
11–50 employees
Short description
Quince Therapeutics is a NASDAQ-listed, late-stage rare disease biotech developing drug/device therapies based on its proprietary AIDE red blood cell encapsulation platform, with a lead Phase 3-failed asset (eDSP) and a newly acquired inhaled rapamycin program (LAM-001) for pulmonary disorders.
Ownership category
akta.pro rank

Quince Therapeutics industry classification

Industry
Product category
Rare Disease Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Medicinal and Botanical Manufacturing (325411)
SIC
Pharmaceutical Preparations (2834), Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
CRISPR & Functional Genomics Screening Platforms (pooled/arrayed screens, perturb-seq) (HLAAAIAG)

Keywords

  • Rare disease therapeutics
  • Drug delivery platform
  • Red blood cell encapsulation
  • Autologous drug device combination
  • Clinical stage biotechnology

Where Quince Therapeutics is headquartered

Location

Headquarters

HQ city
South San Francisco
HQ country
United States
HQ region
North America

Markets served

Quince 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. No current revenue: Quince Therapeutics reports no revenue. The company is pre-commercial, with a negative EPS of -10.62 (as of May 2026) and product candidates still in clinical development or recently failed trials.
  2. Future licensing royalties (planned): The Pipeline page invites inbound licensing inquiries via [email protected] for eDSP across additional indications (DMD and prioritized rare disease targets such as autoimmune hepatitis, pulmonary sarcoidosis, dermatomyositis, pemphigus vulgaris, Hashimoto's encephalopathy, Becker muscular dystrophy, pediatric lupus, juvenile idiopathic arthritis, myasthenia gravis, limb-girdle muscular dystrophy, and chronic inflammatory demyelinating polyradiculoneuropathy). Implies a future licensing/royalty revenue model contingent on regulatory approval.

Go-to-market motion2 records

Quince Therapeutics product offering

Product offering

Core offering

Quince Therapeutics is a late-stage, pre-commercial biotechnology company developing drug/device combination therapeutics for rare diseases using its proprietary AIDE (Autologous Intracellular Drug Encapsulation) platform. The AIDE platform pairs the CE-marked RCL (Red Cell Loader) automated device with a CE-marked sterile single-use treatment kit to encapsulate drugs inside a patient's own red blood cells at the point of care in approximately two hours. Its lead clinical-stage product eDSP (encapsulated dexamethasone sodium phosphate) is being developed for Ataxia-Telangiectasia and Duchenne Muscular Dystrophy, and the company added the inhaled rapamycin product LAM-001 for rare pulmonary disorders via its May 2026 acquisition of Orphai Therapeutics.

Product overview

Quince Therapeutics operates a single integrated product architecture centered on its proprietary AIDE (Autologous Intracellular Drug Encapsulation) technology platform, which pairs the CE-marked RCL (Red Cell Loader) automated device with a CE-marked single-use treatment kit to encapsulate drugs into a patient's own red blood cells at the point of care. The lead clinical-stage product eDSP (encapsulated dexamethasone sodium phosphate, formerly EryDex, acquired via the 2023 EryDel acquisition) is the first drug to leverage this platform, with clinical programs in Ataxia-Telangiectasia (lead indication, Phase 3 NEAT failed in February 2026) and Duchenne Muscular Dystrophy (second indication, Phase 2 study designs finalized). The platform architecture and underlying RCL/EryKit consumables support broader indication expansion (autoimmune hepatitis, pulmonary sarcoidosis, dermatomyositis, pemphigus vulgaris, Hashimoto's encephalopathy, Becker muscular dystrophy, pediatric lupus, juvenile idiopathic arthritis, myasthenia gravis, limb-girdle muscular dystrophy, and chronic inflammatory demyelinating polyradiculoneuropathy). In May 2026 Quince expanded its portfolio through the acquisition of Orphai Therapeutics, adding the inhaled rapamycin product LAM-001 for rare pulmonary disorders (PAH and PH-ILD). The 2022 Novosteo acquisition and corporate rebrand from Cortexyme to Quince Therapeutics completed the pipeline focus on rare-disease therapeutics.

Differentiator

Problem solved

Functional benefit

Brands

  • AIDE (Autologous Intracellular Drug Encapsulation): Proprietary drug/device combination technology platform that encapsulates drugs into a patient's own red blood cells using the RCL device and single-use treatment kit.
  • eDSP

Products and services

  • AIDE Technology Platform (Autologous Intracellular Drug Encapsulation) Proprietary drug/device combination platform that uses an automated process to encapsulate a drug into a patient's own red blood cells, designed to harness benefits including potentially better tolerability, enhanced tissue biodistribution, reduced immunogenicity, and prolongation of circulating half-life; applicable to small molecules, large molecules, peptides, proteins, and biologics.
  • eDSP (encapsulated Dexamethasone Sodium Phosphate; previously EryDex) First product leveraging the AIDE technology platform, composed of dexamethasone sodium phosphate (DSP) encapsulated in autologous red blood cells; designed to maintain corticosteroid efficacy while reducing or eliminating chronic toxicity such as adrenal suppression, with lead development in Ataxia-Telangiectasia and Duchenne Muscular Dystrophy.
  • RCL (Red Cell Loader) Device Proprietary CE-marked non-invasive automated device that performs blood processing at the point of care to automate the AIDE encapsulation process; features a touchscreen interface with three microprocessor circuit boards and handles blood, drug, and processing solutions using the single-use treatment kit.
  • Single-Use Treatment Kit (EryKit consumables) CE-marked sterile, single-use, pyrogen-free disposable blood tubing system used with the RCL to encapsulate small molecules, large molecules, and biologics into human red blood cells; contains a centrifuge, hemoconcentrator filter, bags, organizer cassette, and accessories.
  • LAM-001 (inhaled formulation of rapamycin) Inhaled formulation of rapamycin targeting rare pulmonary disorders including Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension associated with Interstitial Lung Disease (PH-ILD); holds U.S. and EU orphan drug designations across multiple indications.

Companies that use Quince Therapeutics

Customer profile

Ideal customer profiles2 records

Quince Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Quince Therapeutics partnerships and signals

Strategic signal

Recent moves6 records

Expansion highlights5 records

Quince Therapeutics competitors and assessment

Company assessment

Direct peers

  • Liquidia Technologies: Commercial-stage company with YUTREPIA, an inhaled treprostinil for PAH/PH-ILD, putting it in direct therapeutic-area competition with Quince's LAM-001 program.
  • EryTech Pharma: French biotech that develops red blood cell-encapsulated therapeutics (eryaspase, Graspa) — historically the closest direct peer to Quince's AIDE red-cell encapsulation platform, focused on rare metabolic and oncology indications.
  • Gossamer Bio: Late-stage clinical biotech developing seralutinib for PAH; a direct competitor in the rare pulmonary hypertension space where LAM-001 is being positioned.

Broad incumbents

  • Ultragenyx Pharmaceutical: Established rare-disease biotech with multiple approved products and a broad rare-disease pipeline; a natural strategic acquirer/partner comparable for Quince given its rare-disease focus and clinical-stage assets.
  • United Therapeutics: Commercial leader in PAH (Tyvaso, Remodulin, Orenitram) and a key competitor for any inhaled pulmonary asset; relevant comparator for LAM-001's commercial potential in PAH and PH-ILD.
  • BioMarin Pharmaceutical: Major rare-disease commercial player (Naglazyme, Vimizim, Voxzogo, Roctavian) with a long history of orphan drug development and acquisitions of late-stage rare-disease assets — relevant benchmark and potential acquirer profile.
  • Alexion (AstraZeneca Rare Disease): Established rare-disease franchise within AstraZeneca (Soliris, Ultomiris, Strensiq); a benchmark for rare-disease commercial execution and a potential acquirer/partner for AIDE-derived programs.
  • Swedish Orphan Biovitrum (Sobi): Specialty rare-disease biopharma with a portfolio that includes corticosteroids and inflammatory/immunology indications overlapping with the eDSP pipeline expansion list (DMD, JIA, autoimmune diseases).

Emerging players

  • Edgewise Therapeutics: Clinical-stage biotech focused on rare muscle disorders including Duchenne and Becker muscular dystrophy — directly comparable for Quince's eDSP DMD/Becker MD programs.
  • Insmed: Rare pulmonary-disease biotech (approved ARIKAYCE for MAC lung disease and a Phase 3 program in PH-ILD); comparable business model and therapeutic focus to LAM-001's PAH/PH-ILD positioning.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Quince Therapeutics social profiles

Digital presence

Quince Therapeutics compliance and trust

Trust signal

Compliance4 records

Quince Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Quince Therapeutics leadership team

Management profile

Number of profiles

Profiles7 records

Quince Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Quince Therapeutics funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors30 records

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

Quince Therapeutics M&A and investment

M&A and investment

M&A3 records

Investments

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

Frequently asked questions about Quince Therapeutics

What does Quince Therapeutics do?

Quince Therapeutics is a late-stage, pre-commercial biotechnology company developing drug/device combination therapeutics for rare diseases using its proprietary AIDE (Autologous Intracellular Drug Encapsulation) platform. The AIDE platform pairs the CE-marked RCL (Red Cell Loader) automated device with a CE-marked sterile single-use treatment kit to encapsulate drugs inside a patient's own red blood cells at the point of care in approximately two hours. Its lead clinical-stage product eDSP (encapsulated dexamethasone sodium phosphate) is being developed for Ataxia-Telangiectasia and Duchenne Muscular Dystrophy, and the company added the inhaled rapamycin product LAM-001 for rare pulmonary disorders via its May 2026 acquisition of Orphai Therapeutics.

Is Quince Therapeutics a public or private company?

Quince Therapeutics is a public company. It is classified as public and is currently operating.

When was Quince Therapeutics founded?

Quince Therapeutics was founded in 2022. It employs 11 to 50 people.

Where is Quince Therapeutics based?

Quince Therapeutics is headquartered in South San Francisco, United States, in the North America region.

How does Quince Therapeutics make money?

Two revenue lines are on record. No current revenue is the primary driver. The others are future licensing royalties (planned).

Who are Quince Therapeutics's main competitors?

Direct peers on record are Liquidia Technologies, EryTech Pharma and Gossamer Bio. Broad incumbents are Ultragenyx Pharmaceutical, United Therapeutics, BioMarin Pharmaceutical, Alexion (AstraZeneca Rare Disease) and Swedish Orphan Biovitrum (Sobi). Emerging players are Edgewise Therapeutics and Insmed.

Does Quince Therapeutics have an API?

No public API is recorded for Quince Therapeutics.

What industry is Quince Therapeutics in?

Quince Therapeutics's product category is Rare Disease Biopharmaceuticals. Its primary akta.pro industry code is HLAAAIAG, CRISPR & Functional Genomics Screening Platforms (pooled/arrayed screens, perturb-seq). Its NAICS code is 325414 and its SIC code is 2834.

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Live signals
Ticker ReportQuince Therapeutics Stockholders Approve PIPE, Share Increase and Equity PlansQuince Therapeutics stockholders approved five proposals at its Oct. 6, 2026 special meeting, including conversion of preferred stock, a PIPE, and an increase in authorized shares. The proposals would issue more than 20% of outstanding common stock and trigger a change of control. Final voting results will be filed with the SEC within four business days.Seeking AlphaQuince Therapeutics, Inc. (QNCX) Discusses LAM-001 Clinical Progress in Pulmonary Hypertension and Bronchiolitis Obliterans Syndrome TranscriptQuince Therapeutics discussed its LAM-001 inhaled rapamycin program, which is advancing into a Phase IIb study for pulmonary hypertension in interstitial lung disease. The company expects data from this study in the first quarter of 2028, following promising Phase IIa results.American Banking and Market NewsQuince Therapeutics (NASDAQ:QNCX) Research Coverage Started at Rodman & RenshawRodman & Renshaw initiated coverage on Quince Therapeutics with a buy rating and $70 target. The stock opened at $31, and the company reported a loss of $12.31 per share, beating the consensus estimate of $28.02. Analysts have a consensus rating of Moderate Buy with an average target of $206.71.Markets DailyQuince Therapeutics (NASDAQ:QNCX) Upgraded at Citizens JmpCitizens JMP upgraded Quince Therapeutics to an outperform rating with a $77 price objective. The stock opened at $30, and the company reported a loss of $12.31 EPS, beating estimates. Analysts have a consensus Moderate Buy with an average price target of $206.71.Quiver QuantitativeQuince Therapeutics to Participate in September 2026 Investor Conferences | QNCX Stock NewsQuince Therapeutics announced senior management participation in September 2026 investor conferences, including a fireside chat on September 9 and a presentation on September 14. The company is developing LAM-001 for pulmonary hypertension, with ongoing Phase 2 studies and a Phase 2 trial in sarcoidosis-associated pulmonary hypertension anticipated in late 2026.American Banking and Market NewsQuince Therapeutics, Inc. (NASDAQ:QNCX) Receives $260.00 Average Price Target from AnalystsMarketbeat Ratings reports that twelve analysts covering Quince Therapeutics (NASDAQ:QNCX) have given the stock an average "Hold" rating, with a one-year average target price of $260.00. The stock opened at $33.75, trading above its 50-day and 200-day moving averages, and reported quarterly EPS of ($12.31) versus a consensus of ($28.02).FierceBiotechChutes & Ladders—Vivace revs up C-suite ahead of pivotal pushVivace Therapeutics named Craig Gibbs, Ph.D., president and CEO and Ellen Lubman chief business and strategy officer ahead of advancing its mesothelioma candidate VT3989 into a phase 3 registrational trial, granted Fast Track and Orphan Drug designations. Other moves include Mirai Bio's Kate Torchilin becoming permanent CEO, Rhythm's Manher Joshi as CMO, and Quince president Charles Ryan departing September 8.Quiver Quantitative$QSI stock is up 18% today. Here's what we see in our data. | QSI Stock NewsQuince Therapeutics (QSI) stock rose 18% on a trading volume of approximately $4.5 million, driven by recent insider buying activity and shifting institutional sentiment. Despite the price increase, the company reported a 41.79% decline in Q2 2026 revenue to $344K, while major institutional investors like BlackRock and State Street significantly reduced their holdings.Markets DailyQuince Therapeutics’ (QNCX) “Overweight” Rating Reiterated at Cantor FitzgeraldCantor Fitzgerald reiterated an overweight rating on Quince Therapeutics with a $70.00 price target, joining other analysts who have recently adjusted their views on the biopharmaceutical company. Institutional investors, including Nantahala Capital Management and Vanguard Group, significantly increased their stakes in the firm during recent quarters.BioWorldQuince’s eDSP on ice after Neat phase III fails in A-TQuince Therapeutics Inc. has discontinued development of its eDSP treatment for ataxia-telangiectasia following the failure of the Neat phase III clinical trial. Analysts indicate that this setback effectively removes the company's core value driver, resulting in a full impairment of the equity.