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Serapha Bio

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uuid02lw7hy

Namestring
Serapha Bio
Legal namestring
Serapha Bio Inc.
Websiteurl
seraphabio.com
Company typeenum
Private
Founded yearint
2026
Operating statusenum
Operating
Ownership categoryenum
akta.pro rankint
HeadquartersNew York, United States
HQ citystring
New York
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
base editing therapy, gene editing biotechnology, rare disease therapeutics, alpha-1 antitrypsin treatment, clinical stage biopharmaceutical
Industry1 code
1Gene Therapy for Rare/Monogenic Diseases
CodeHLAAACAEPrimaryYes
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Gene Editing Therapeutics
No data
Revenue model1 record
1Not yet commercial
TypeSubscription Recurring
Description

Serapha Bio is a pre-commercial biotech company. The company has not yet generated product revenue and appears to be in the development stage, pending the completion of its merger with Boundless Bio.

seraphabio.com
Cost components3 values
Technology or R&D, Personnel, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Serapha Bio is a clinical-stage biotechnology company developing a base-editing gene therapy to treat Alpha-1 Antitrypsin Deficiency, a rare genetic disorder caused by mutations in the SERPINA1 gene. The company's lead therapeutic candidate employs base-editing technology to correct the disease-causing mutation, with the intent to provide a disease-modifying treatment for affected patients.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Serapha Bio is a biotech company. The source data does not provide specific details on its product portfolio, platform architecture, or individual product/module names. The company announced a merger agreement with Boundless Bio with a concurrent $230 million private placement.

Product and service1 record
1Base-editing therapy for Alpha-1 Antitrypsin Deficiency
CategoryGene Editing Therapeutics
Description

An investigational base-editing gene therapy designed to correct the SERPINA1 gene mutation causing Alpha-1 Antitrypsin Deficiency. It is intended for patients with this rare hereditary disorder characterized by lung and liver disease.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2026-06-23
Description

Serapha Bio announced a definitive merger agreement with Boundless Bio Inc on June 23, 2026. The transaction includes a concurrent private placement of $230 million. This is the company's primary strategic transaction, representing a merger of two biotech entities.

Recent move3 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight3 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

CRISPR Therapeutics is the first commercial-stage CRISPR/Cas9 gene-editing company (Casgevy approval) with a broad pipeline including liver-directed and rare-disease programs. It is a broad incumbent in the gene-editing space relevant to Serapha's monogenic disease focus.

TypeBroad incumbent
Description

Sangamo Therapeutics is a clinical-stage genomic medicine company with zinc finger nuclease-based in vivo genome editing programs including liver-directed monogenic disease therapies. As a broad incumbent in genomic medicine, it represents both a peer and a potential acquisition target/partnership candidate.

TypeEmerging player
Description

Wave Life Sciences is a clinical-stage genetic medicines company developing RNA editing (PRISM platform) and antisense oligonucleotides for rare diseases including AATD-adjacent indications. Its RNA-editing modality overlaps with Serapha's gene-editing approach to monogenic disease.

TypeDirect peer
Description

Korro Bio is developing RNA editing (ADAR-mediated) therapies for rare diseases including Alpha-1 Antitrypsin Deficiency — directly targeting the same indication as Serapha. Although the modality (RNA editing vs base editing) differs, the indication, delivery, and patient population are essentially identical.

TypeDirect peer
Description

Prime Medicine is a clinical-stage company developing prime editing, a next-generation gene-editing modality closely related to base editing. Both target precise correction of disease-causing mutations in genetic disorders, making Prime a direct platform peer to Serapha's base-editing approach.

TypeEmerging player
Description

CAMP4 Therapeutics is an emerging clinical-stage company developing RNA-based therapeutics that upregulate gene expression to treat rare genetic diseases. While targeting a different mechanism (expression enhancement vs editing), it competes for the same patient populations and rare liver/genetic disease space.

TypeDirect peer
Description

Verve Therapeutics develops in vivo base-editing and gene-editing therapies delivered via lipid nanoparticles, primarily for cardiovascular disease but with platform overlap in liver-directed monogenic disease editing. Directly comparable to Serapha's LNP-delivered base-editing approach.

TypeBroad incumbent
Description

Editas Medicine is a clinical-stage gene-editing company developing CRISPR/Cas9 and Cas12a therapies for rare genetic diseases. It operates broadly in the same gene-editing category as Serapha Bio and competes for talent, partnerships, and clinical development talent.

TypeDirect peer
Description

Beam Therapeutics is the leading clinical-stage base-editing platform company, developing in vivo and ex vivo base-editing therapies for rare and serious diseases. It is the closest direct peer to Serapha Bio given identical base-editing modality and shared focus on monogenic liver-directed disorders.

TypeBroad incumbent
Description

Intellia is a clinical-stage CRISPR/Cas9 gene-editing company with programs in liver-directed in vivo editing (NTLA-2001 for ATTR amyloidosis) and other monogenic diseases. As a broader gene-editing incumbent, it competes for the same liver-target patient populations and editing modality space.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 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 highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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 maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
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

Investors11 records

Each record includes

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

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

M&A1 record

Each record includes

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

Investment

Each record includes

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

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

Serapha Bio

Gene Editing Therapeuticsseraphabio.com

Serapha Bio firmographics

Firmographics
Name
Serapha Bio
Legal name
Serapha Bio Inc.
Website
https://seraphabio.com
Company type
Private
Founded year
2026
Operating status
Operating
Ownership category
akta.pro rank

Serapha Bio industry classification

Industry
Product category
Gene Editing Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Gene Therapy for Rare/Monogenic Diseases (HLAAACAE)

Keywords

  • Base editing therapy
  • Gene editing biotechnology
  • Rare disease therapeutics
  • Alpha-1 antitrypsin treatment
  • Clinical stage biopharmaceutical

Where Serapha Bio is headquartered

Location

Headquarters

HQ city
New York
HQ country
United States
HQ region
North America

Markets served

Serapha Bio business model

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

Revenue model

  1. Not yet commercial: Serapha Bio is a pre-commercial biotech company. The company has not yet generated product revenue and appears to be in the development stage, pending the completion of its merger with Boundless Bio.

Serapha Bio product offering

Product offering

Core offering

Serapha Bio is a clinical-stage biotechnology company developing a base-editing gene therapy to treat Alpha-1 Antitrypsin Deficiency, a rare genetic disorder caused by mutations in the SERPINA1 gene. The company's lead therapeutic candidate employs base-editing technology to correct the disease-causing mutation, with the intent to provide a disease-modifying treatment for affected patients.

Product overview

Serapha Bio is a biotech company. The source data does not provide specific details on its product portfolio, platform architecture, or individual product/module names. The company announced a merger agreement with Boundless Bio with a concurrent $230 million private placement.

Differentiator

Problem solved

Functional benefit

Products and services

  • Base-editing therapy for Alpha-1 Antitrypsin Deficiency An investigational base-editing gene therapy designed to correct the SERPINA1 gene mutation causing Alpha-1 Antitrypsin Deficiency. It is intended for patients with this rare hereditary disorder characterized by lung and liver disease.

Companies that use Serapha Bio

Customer profile

Ideal customer profiles1 record

Serapha Bio technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Serapha Bio partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Boundless Bio IncflagshipStrategic or Co-development Partner · 23 June 2026Serapha Bio announced a definitive merger agreement with Boundless Bio Inc on June 23, 2026. The transaction includes a concurrent private placement of $230 million. This is the company's primary strategic transaction, representing a merger of two biotech entities.

Scale indicators2 records

Recent moves3 records

Expansion highlights3 records

Serapha Bio competitors and assessment

Company assessment

Broad incumbents

  • CRISPR Therapeutics: CRISPR Therapeutics is the first commercial-stage CRISPR/Cas9 gene-editing company (Casgevy approval) with a broad pipeline including liver-directed and rare-disease programs. It is a broad incumbent in the gene-editing space relevant to Serapha's monogenic disease focus.
  • Sangamo Therapeutics: Sangamo Therapeutics is a clinical-stage genomic medicine company with zinc finger nuclease-based in vivo genome editing programs including liver-directed monogenic disease therapies. As a broad incumbent in genomic medicine, it represents both a peer and a potential acquisition target/partnership candidate.
  • Editas Medicine: Editas Medicine is a clinical-stage gene-editing company developing CRISPR/Cas9 and Cas12a therapies for rare genetic diseases. It operates broadly in the same gene-editing category as Serapha Bio and competes for talent, partnerships, and clinical development talent.
  • Intellia Therapeutics: Intellia is a clinical-stage CRISPR/Cas9 gene-editing company with programs in liver-directed in vivo editing (NTLA-2001 for ATTR amyloidosis) and other monogenic diseases. As a broader gene-editing incumbent, it competes for the same liver-target patient populations and editing modality space.

Emerging players

  • Wave Life Sciences: Wave Life Sciences is a clinical-stage genetic medicines company developing RNA editing (PRISM platform) and antisense oligonucleotides for rare diseases including AATD-adjacent indications. Its RNA-editing modality overlaps with Serapha's gene-editing approach to monogenic disease.
  • CAMP4 Therapeutics: CAMP4 Therapeutics is an emerging clinical-stage company developing RNA-based therapeutics that upregulate gene expression to treat rare genetic diseases. While targeting a different mechanism (expression enhancement vs editing), it competes for the same patient populations and rare liver/genetic disease space.

Direct peers

  • Korro Bio: Korro Bio is developing RNA editing (ADAR-mediated) therapies for rare diseases including Alpha-1 Antitrypsin Deficiency — directly targeting the same indication as Serapha. Although the modality (RNA editing vs base editing) differs, the indication, delivery, and patient population are essentially identical.
  • Prime Medicine: Prime Medicine is a clinical-stage company developing prime editing, a next-generation gene-editing modality closely related to base editing. Both target precise correction of disease-causing mutations in genetic disorders, making Prime a direct platform peer to Serapha's base-editing approach.
  • Verve Therapeutics: Verve Therapeutics develops in vivo base-editing and gene-editing therapies delivered via lipid nanoparticles, primarily for cardiovascular disease but with platform overlap in liver-directed monogenic disease editing. Directly comparable to Serapha's LNP-delivered base-editing approach.
  • Beam Therapeutics: Beam Therapeutics is the leading clinical-stage base-editing platform company, developing in vivo and ex vivo base-editing therapies for rare and serious diseases. It is the closest direct peer to Serapha Bio given identical base-editing modality and shared focus on monogenic liver-directed disorders.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights5 records

Customer concentration

Serapha Bio financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Serapha Bio leadership team

Management profile

Number of profiles

Serapha Bio funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors11 records

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

Serapha Bio M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about Serapha Bio

What does Serapha Bio do?

Serapha Bio is a clinical-stage biotechnology company developing a base-editing gene therapy to treat Alpha-1 Antitrypsin Deficiency, a rare genetic disorder caused by mutations in the SERPINA1 gene. The company's lead therapeutic candidate employs base-editing technology to correct the disease-causing mutation, with the intent to provide a disease-modifying treatment for affected patients.

Is Serapha Bio a public or private company?

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

When was Serapha Bio founded?

Serapha Bio was founded in 2026.

Where is Serapha Bio based?

Serapha Bio is headquartered in New York, United States, in the North America region.

How does Serapha Bio make money?

One revenue line is on record: not yet commercial.

Who are Serapha Bio's main competitors?

Broad incumbents on record are CRISPR Therapeutics, Sangamo Therapeutics, Editas Medicine and Intellia Therapeutics. Emerging players are Wave Life Sciences and CAMP4 Therapeutics. Direct peers are Korro Bio, Prime Medicine, Verve Therapeutics and Beam Therapeutics.

Does Serapha Bio have an API?

No public API is recorded for Serapha Bio.

What industry is Serapha Bio in?

Serapha Bio's product category is Gene Editing Therapeutics. Its primary akta.pro industry code is HLAAACAE, Gene Therapy for Rare/Monogenic Diseases. Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
BioPharma DiveBeam sues 2 biotechs, alleging theft of base editing trade secretsBeam Therapeutics sued YolTech Therapeutics and Serapha Bio, alleging a former employee stole base-editing trade secrets to develop an AATD treatment. Beam seeks to stop misuse and recover value from the undisclosed upfront payment. Serapha plans a Phase 2/3 trial later this year or early 2027.BostonGlobe.comBeam Therapeutics sues Chinese biotech, VC-backed startup, alleging theft of intellectual propertyBeam Therapeutics sued former scientist Zi Jun Wang and Chinese company YolTech Therapeutics, alleging Wang stole intellectual property to found YolTech, which co-founded Serapha Bio with VC firms. The lawsuit centers on Beam's base-editing treatment for AATD, with YolTech contesting the claims.Investing.comRTW Biotech Opportunities reports 9.7% June NAV increase By Investing.comRTW Biotech Opportunities Ltd reported its net asset value per ordinary share reached $2.86 as of June 30, representing a 9.7% monthly increase that matched the Nasdaq Biotech Index but trailed the Russell 2000 Biotech Index's 15.8% gain. The company's top holdings include CG Oncology (7.2% of NAV), UroGen (6.8%), and Kailera Therapeutics (5.9%), while it made new investments of $1.4 million in Lycia Therapeutics and $7.5 million in Serapha Bio. During the quarter, AbbVie announced the acquisition of portfolio company Apogee Therapeutics for approximately $10.9 billion, prompting RTW Bio to close its Apogee position.Investing.comRTW Biotech Opportunities reports 9.7% June NAV increase By Investing.comRTW Biotech Opportunities Ltd reported its net asset value per ordinary share reached $2.86 as of June 30, representing a 9.7% increase from the previous month, matching the Nasdaq Biotech Index's return but trailing the Russell 2000 Biotech Index's 15.8% advance. The company invested $1.4 million in Lycia Therapeutics as part of a $75 million Series D financing round and $7.5 million in Serapha Bio's Series A financing, with an additional $7.5 million planned pending Serapha Bio's merger with Boundless Bio. Over the twelve months ending June 30, RTW Bio repurchased 7.6 million shares for $14.4 million, with the discount to NAV narrowing from 28.8% to 15.4%.FinancialContent Business PageHalper Sadeh LLC is Investigating Whether DAN, ESI, NUVL, BOLD are Obtaining Fair Deals for their ShareholdersHalper Sadeh LLC, an investor rights law firm, announced investigations into four proposed corporate transactions for potential violations of federal securities laws and breaches of fiduciary duties to shareholders. The transactions include Dana Incorporated's sale to Eaton Corporation plc, Element Solutions Inc's sale to Solstice Advanced Materials Inc for $10.00 cash plus 0.500 shares per share, Nuvalent Inc's sale to GSK plc for $124.00 per share, and Boundless Bio Inc's merger with Serapha Bio Inc. The law firm is inviting shareholders of these companies to discuss their legal rights and options at no cost.GlobeNewswireHalper Sadeh LLC is Investigating Whether DAN, ESI, NUVL, BOLD are Obtaining Fair Deals for their ShareholdersInvestor rights law firm Halper Sadeh LLC announced it is investigating whether Dana Incorporated, Element Solutions Inc, Nuvalent Inc, and Boundless Bio Inc obtained fair deals for shareholders in their respective proposed transactions. The four proposed deals involve sales or mergers with Eaton Corporation plc, Solstice Advanced Materials Inc, GSK plc, and Serapha Bio Inc respectively, with shareholder ownership stakes in combined companies ranging from approximately 3.7% to 49.9%. The law firm is reaching out to shareholders to discuss potential legal rights and remedies, including seeking increased consideration or additional disclosures.MorningstarSHAREHOLDER ALERT: The M&A Class Action Firm Continues to Investigate the Merger—ACA, APGE, BOLD, and GBCSMonteverde & Associates PC is investigating four M&A deals: Arcosa's sale to CRH Americas, Apogee's sale to AbbVie, Boundless Bio's merger with Serapha Bio, and Selectis Health's sale to Black Pearl Equities. The proposed transactions offer $150, $135.11, a 3.7% stake, and $5.75 per share respectively.Tech TimesAlpha-1 Antitrypsin Gene Editing Startup Raises $230 Million: Serapha Bio AATD DebutSerapha Bio emerged from stealth on June 23, 2026 with $230 million in financing and a base-editing therapy for alpha-1 antitrypsin deficiency. The therapy, SERP-01, has human proof-of-concept data and cleared US regulatory review, targeting a single mutation shared by over 95% of severe cases. The company plans a reverse merger with Boundless Bio, trading as AATD, with Phase 3 trials expected in 2029.PR NewswireAre TECH, APGE, BOLD, REFI Obtaining Fair Deals for their Shareholders?Halper Sadeh LLC, an investor rights law firm, announced investigations into four proposed M&A transactions for potential violations of federal securities laws and breaches of fiduciary duties to shareholders. The transactions include Bio-Techne Corporation's sale to Merck KGaA for $73.00 per share, Apogee Therapeutics' sale to AbbVie for $135.11 per share, Boundless Bio's merger with Serapha Bio, and Chicago Atlantic Real Estate Finance's merger with Chicago Atlantic BDC. The law firm stated it may seek increased consideration, additional disclosures, or other relief on behalf of shareholders.GlobeNewswireThese Emerging Companies Are Racing Toward Major CatalystsThis 24/7 Market News article profiles four emerging companies approaching significant near-term catalysts: NeOnc Technologies received Investigational New Drug authorization from the Department of Health–Abu Dhabi for its NEO100 program targeting high-grade gliomas, with Phase 2a readout expected by end of July 2026; Boundless Bio announced a merger with privately held Serapha Bio and approximately $230 million in committed financing from RTW Investments and RA Capital Management for gene-editing therapies targeting Alpha-1 Antitrypsin Deficiency; Backblaze secured a five-year, multi-exabyte data storage agreement valued at approximately $335 million with CoreWeave supporting AI cloud infrastructure; and HeartSciences proposed a business combination with Fortitude Mining Holdings, a digital asset mining platform backed by Digital Currency Group expected to hold approximately 95% of the combined entity.