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Connect Biopharma

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uuid00q6vm7

Namestring
Connect Biopharma
Legal namestring
Connect Biopharma Holdings Limited
Company typeenum
Public
Founded yearint
2012
Descriptiontext

Connect Biopharma Holdings Limited (NASDAQ: CNTB) is a clinical-stage biopharmaceutical company headquartered in San Diego, California, with operations in the U.S. and China (Taicang R&D facility). The company is focused on developing next-generation antibody therapies for inflammatory diseases, principally type-2 inflammation-driven conditions including asthma, chronic obstructive pulmonary disease (COPD), and atopic dermatitis.

The company's lead product candidate is rademikibart (formerly CBP-201), a next-generation monoclonal antibody targeting interleukin-4 receptor alpha (IL-4Rα). By blocking IL-4Rα, rademikibart inhibits both IL-4 and IL-13 signaling, the central drivers of type-2 inflammation. It has demonstrated clinical activity in both atopic dermatitis (Phase 2b completed; partner Simcere has completed a Phase 3 in China with an NDA pending) and asthma (global Phase 2b completed), and Phase 1 data showed rapid FEV1 improvements of 100–400 mL as early as 15 minutes post-dosing, a profile that positions the asset for the acute exacerbation setting rather than purely chronic maintenance. A second pipeline candidate, icanbelimod (CBP-307), is in development for ulcerative colitis.

Connect Biopharma is pre-revenue (Q1 2026 revenue approximately ($0.05 million)) and monetizes today primarily through licensing. It holds an exclusive Greater China license with Simcere Pharmaceutical — worth up to $110 million in potential milestones plus tiered royalties on net sales — and is seeking a commercial partner for broader inflammatory disease commercialization. The company funded operations into the second half of 2027 following a $20.2 million private placement in March 2026 led by Panacea Venture. Estimated hospital pricing for rademikibart of $600–$700 per dose compares with Dupixent's approximately $3,800 per month, signaling a potential cost-advantage thesis at launch. Go-to-market activities center on investor conferences, medical conference presentations, and disease-awareness partnerships ahead of any U.S. approval.

Short descriptiontext

Connect Biopharma (NASDAQ: CNTB) is a clinical-stage biopharmaceutical company developing rademikibart, a next-generation anti-IL-4Rα antibody for acute asthma and COPD exacerbations and atopic dermatitis, with a secondary candidate icanbelimod for ulcerative colitis. It monetizes via an exclusive Greater China license to Simcere Pharmaceutical while seeking a broader commercial partner.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
inflammatory disease therapeutics, biopharmaceutical drug development, monoclonal antibody therapies, asthma COPD treatments, atopic dermatitis biologics
Industry4 codes
1Respiratory & Allergy Pharmaceuticals
CodeHLAIAAAHPrimaryYes
2Immunology & Autoimmune Specialty Pharmaceuticals
CodeHLAIACABPrimaryNo
3Immunology & Inflammation Pharmaceuticals
CodeHLAIAAADPrimaryNo
4Dermatology Specialty Pharmaceuticals
CodeHLAIACALPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Biopharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Drug Development and Commercialization
TypeSubscription Recurring
Description

Pre-revenue clinical-stage biopharma company developing rademikibart for asthma, COPD, and atopic dermatitis. Expected to fund operations into second half of 2027 with current cash reserves.

investors.connectbiopharma.com
2Licensing Revenue - Simcere Partnership
TypeLicensing Royalties
Description

Exclusive license agreement with Simcere Pharmaceutical for rademikibart in Greater China with potential milestone payments of up to $110 million plus tiered royalties on net sales. Simcere has an NDA pending with potential H2 approval triggering milestone payments.

stocktitan.net
Marketing channels3 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, Marketing or Sales, Operations, Supply Chain
Pricing details1 tier
1Estimated hospital pricing for rademikibart
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Early payer work suggesting hospital pricing of $600-$700 per dose compared to DUPIXENT's ~$3,800/month

finance.yahoo.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Connect Biopharma is a clinical-stage biopharmaceutical company developing rademikibart, a next-generation anti-IL-4Rα antibody designed to treat acute asthma and COPD exacerbations as well as atopic dermatitis. The company also has icanbelimod (CBP-307) in its pipeline for ulcerative colitis. It licenses rademikibart to Simcere Pharmaceutical for Greater China and is pre-revenue.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Rapid FEV1 improvements of 100-400 mL as early as 15 minutes post-dosing maintained through Day 29 in Phase 1 study
+2 more records
Product overview1 text field

Connect Biopharma is a clinical-stage biopharmaceutical company dedicated to transforming care for asthma and COPD. The company's lead product candidate is rademikibart (formerly CBP-201), a next-generation antibody targeting interleukin-4 receptor alpha (IL-4Rα). The company is also developing icanbelimod (CBP-307) for ulcerative colitis. Connect Biopharma operates with global operations spanning the U.S. and China, and maintains an exclusive license agreement with Simcere Pharmaceutical for rademikibart in Greater China.

Product and service2 records
1Rademikibart (CBP-201)
CategoryLead Product Candidate
Description

A next-generation anti-IL-4Rα antibody targeting interleukin-4 receptor alpha to treat acute asthma and COPD exacerbations and atopic dermatitis, intended for healthcare providers and biopharma licensees.

2Icanbelimod (CBP-307)
CategoryProduct Candidate
Description

An investigational therapy being evaluated for ulcerative colitis treatment as part of Connect Biopharma's pipeline of inflammatory disease treatments.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2026-04-13
Description

Corporate partnership with the Jovante Woods Foundation (founded by NFL legend Ickey Woods) to accelerate asthma testing and educational programs for children nationwide through the 'Score 6 for 24' fundraising campaign.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2026-03-30
Description

Exclusive license agreement with Simcere Pharmaceutical for rademikibart in Greater China worth up to $110 million in potential milestone payments plus tiered royalties on net sales. Simcere conducted Phase 3 study of rademikibart for moderate-to-severe atopic dermatitis in China, with NDA pending and potential H2 2026 approval triggering milestone payments.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Markets Tezspire (tezepelumab) and Fasenra (benralizumab) in severe asthma and has expanded respiratory biologic offerings, making it a direct competitor in the type 2 inflammation and severe asthma segments where rademikibart is positioned.

TypeDirect peer
Description

Commercializes Dupixent alongside Regeneron and is the dominant player in the atopic dermatitis and asthma biologic markets rademikibart is targeting. Highly comparable as the established incumbent in the same disease areas with overlapping IL-4Rα positioning.

TypeDirect peer
Description

Markets Nemluvio (nemolizumab) for atopic dermatitis and prurigo nodularis, directly competing with rademikibart's atopic dermatitis indication. Comparable as a dermatology-focused immunology biologic peer.

TypeBroad incumbent
Description

Markets Cibinqo (abrocitinib) and Eucrisa in atopic dermatitis, as well as broader respiratory and inflammation assets. Comparable as a broad incumbent in the inflammatory dermatology and respiratory disease categories overlapping with rademikibart's indications.

TypeDirect peer
Description

Co-developer of Tezspire (tezepelumab) with AstraZeneca for severe asthma, directly competing with rademikibart's planned acute asthma positioning and overlapping with rademikibart's type 2 inflammation focus.

TypeDirect peer
Description

Markets Xolair (omalizumab) for allergic asthma and other inflammatory indications, competing in the same physician-prescribed biologic asthma space that rademikibart targets with its anti-IL-4Rα approach.

TypeBroad incumbent
Description

Markets Olumiant (baricitinib, JAK inhibitor) and Taltz in inflammatory diseases including atopic dermatitis and asthma-adjacent indications. Comparable as a broad incumbent in the inflammatory disease space where rademikibart competes.

TypeDirect peer
Description

Markets Nucala (mepolizumab) and Trelegy in asthma and COPD, and has a substantial respiratory biologic franchise overlapping with rademikibart's lead indications. Directly comparable as an established respiratory immunology competitor.

TypeEmerging player
Description

Commercial-stage dermatology company developing topical and biologic therapies for inflammatory skin diseases including atopic dermatitis. Comparable as an emerging immunology/dermatology player with overlapping addressable market, though smaller and focused on topicals.

TypeDirect peer
Description

Co-developer of Dupixent (dupilumab), the leading IL-4Rα antibody and the direct therapeutic competitor to rademikibart in asthma, COPD, and atopic dermatitis. Most directly comparable peer given identical mechanism and overlapping indications.

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 highlights6 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 profile3 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 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 rounds

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 →

Connect Biopharma

Biopharmaceuticalsconnectbiopharma.com

Connect Biopharma (NASDAQ: CNTB) is a clinical-stage biopharmaceutical company developing rademikibart, a next-generation anti-IL-4Rα antibody for acute asthma and COPD exacerbations and atopic dermatitis, with a secondary candidate icanbelimod for ulcerative colitis. It monetizes via an exclusive Greater China license to Simcere Pharmaceutical while seeking a broader commercial partner.

What Connect Biopharma does

Connect Biopharma Holdings Limited (NASDAQ: CNTB) is a clinical-stage biopharmaceutical company headquartered in San Diego, California, with operations in the U.S. and China (Taicang R&D facility). The company is focused on developing next-generation antibody therapies for inflammatory diseases, principally type-2 inflammation-driven conditions including asthma, chronic obstructive pulmonary disease (COPD), and atopic dermatitis.

The company's lead product candidate is rademikibart (formerly CBP-201), a next-generation monoclonal antibody targeting interleukin-4 receptor alpha (IL-4Rα). By blocking IL-4Rα, rademikibart inhibits both IL-4 and IL-13 signaling, the central drivers of type-2 inflammation. It has demonstrated clinical activity in both atopic dermatitis (Phase 2b completed; partner Simcere has completed a Phase 3 in China with an NDA pending) and asthma (global Phase 2b completed), and Phase 1 data showed rapid FEV1 improvements of 100–400 mL as early as 15 minutes post-dosing, a profile that positions the asset for the acute exacerbation setting rather than purely chronic maintenance. A second pipeline candidate, icanbelimod (CBP-307), is in development for ulcerative colitis.

Connect Biopharma is pre-revenue (Q1 2026 revenue approximately ($0.05 million)) and monetizes today primarily through licensing. It holds an exclusive Greater China license with Simcere Pharmaceutical — worth up to $110 million in potential milestones plus tiered royalties on net sales — and is seeking a commercial partner for broader inflammatory disease commercialization. The company funded operations into the second half of 2027 following a $20.2 million private placement in March 2026 led by Panacea Venture. Estimated hospital pricing for rademikibart of $600–$700 per dose compares with Dupixent's approximately $3,800 per month, signaling a potential cost-advantage thesis at launch. Go-to-market activities center on investor conferences, medical conference presentations, and disease-awareness partnerships ahead of any U.S. approval.

Connect Biopharma firmographics

Firmographics
Name
Connect Biopharma
Legal name
Connect Biopharma Holdings Limited
Website
https://connectbiopharma.com
Company type
Public
Founded year
2012
Operating status
Operating
Headcount range
51–100 employees
Short description
Connect Biopharma (NASDAQ: CNTB) is a clinical-stage biopharmaceutical company developing rademikibart, a next-generation anti-IL-4Rα antibody for acute asthma and COPD exacerbations and atopic dermatitis, with a secondary candidate icanbelimod for ulcerative colitis. It monetizes via an exclusive Greater China license to Simcere Pharmaceutical while seeking a broader commercial partner.
Ownership category
akta.pro rank

Connect Biopharma industry classification

Industry
Product category
Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Respiratory & Allergy Pharmaceuticals (HLAIAAAH)
akta.pro secondary industries
Immunology & Autoimmune Specialty Pharmaceuticals (HLAIACAB), Immunology & Inflammation Pharmaceuticals (HLAIAAAD), Dermatology Specialty Pharmaceuticals (HLAIACAL)

Keywords

  • Inflammatory disease therapeutics
  • Biopharmaceutical drug development
  • Monoclonal antibody therapies
  • Asthma COPD treatments
  • Atopic dermatitis biologics

Where Connect Biopharma is headquartered

Location

Headquarters

HQ city
San Diego
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Connect Biopharma business model

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

Revenue model

  1. Drug Development and Commercialization: Pre-revenue clinical-stage biopharma company developing rademikibart for asthma, COPD, and atopic dermatitis. Expected to fund operations into second half of 2027 with current cash reserves.
  2. Licensing Revenue - Simcere Partnership: Exclusive license agreement with Simcere Pharmaceutical for rademikibart in Greater China with potential milestone payments of up to $110 million plus tiered royalties on net sales. Simcere has an NDA pending with potential H2 approval triggering milestone payments.

Pricing tiers

ModelBillingPrice
Unit PricingPay-as-you-goEstimated hospital pricing for rademikibart

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Connect Biopharma product offering

Product offering

Core offering

Connect Biopharma is a clinical-stage biopharmaceutical company developing rademikibart, a next-generation anti-IL-4Rα antibody designed to treat acute asthma and COPD exacerbations as well as atopic dermatitis. The company also has icanbelimod (CBP-307) in its pipeline for ulcerative colitis. It licenses rademikibart to Simcere Pharmaceutical for Greater China and is pre-revenue.

Product overview

Connect Biopharma is a clinical-stage biopharmaceutical company dedicated to transforming care for asthma and COPD. The company's lead product candidate is rademikibart (formerly CBP-201), a next-generation antibody targeting interleukin-4 receptor alpha (IL-4Rα). The company is also developing icanbelimod (CBP-307) for ulcerative colitis. Connect Biopharma operates with global operations spanning the U.S. and China, and maintains an exclusive license agreement with Simcere Pharmaceutical for rademikibart in Greater China.

Differentiator

Problem solved

Functional benefit

Products and services

  • Rademikibart (CBP-201) A next-generation anti-IL-4Rα antibody targeting interleukin-4 receptor alpha to treat acute asthma and COPD exacerbations and atopic dermatitis, intended for healthcare providers and biopharma licensees.
  • Icanbelimod (CBP-307) An investigational therapy being evaluated for ulcerative colitis treatment as part of Connect Biopharma's pipeline of inflammatory disease treatments.

Quantifiable outcome

  • Rapid FEV1 improvements of 100-400 mL as early as 15 minutes post-dosing maintained through Day 29 in Phase 1 study
  • +2 more outcomes

Companies that use Connect Biopharma

Customer profile

Segments3 records

Ideal customer profiles3 records

Connect Biopharma technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Connect Biopharma partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered minor and core.

  • Jovante Woods FoundationminorStrategic or Co-development Partner · 13 April 2026Corporate partnership with the Jovante Woods Foundation (founded by NFL legend Ickey Woods) to accelerate asthma testing and educational programs for children nationwide through the 'Score 6 for 24' fundraising campaign.
  • Simcere PharmaceuticalcoreOEM/ Whitelabel/ Licensing Partner · 30 March 2026Exclusive license agreement with Simcere Pharmaceutical for rademikibart in Greater China worth up to $110 million in potential milestone payments plus tiered royalties on net sales. Simcere conducted Phase 3 study of rademikibart for moderate-to-severe atopic dermatitis in China, with NDA pending and potential H2 2026 approval triggering milestone payments.

Scale indicators5 records

Recent moves6 records

Expansion highlights6 records

Connect Biopharma competitors and assessment

Company assessment

Direct peers

  • AstraZeneca: Markets Tezspire (tezepelumab) and Fasenra (benralizumab) in severe asthma and has expanded respiratory biologic offerings, making it a direct competitor in the type 2 inflammation and severe asthma segments where rademikibart is positioned.
  • Sanofi: Commercializes Dupixent alongside Regeneron and is the dominant player in the atopic dermatitis and asthma biologic markets rademikibart is targeting. Highly comparable as the established incumbent in the same disease areas with overlapping IL-4Rα positioning.
  • Galderma: Markets Nemluvio (nemolizumab) for atopic dermatitis and prurigo nodularis, directly competing with rademikibart's atopic dermatitis indication. Comparable as a dermatology-focused immunology biologic peer.
  • Amgen: Co-developer of Tezspire (tezepelumab) with AstraZeneca for severe asthma, directly competing with rademikibart's planned acute asthma positioning and overlapping with rademikibart's type 2 inflammation focus.
  • Novartis: Markets Xolair (omalizumab) for allergic asthma and other inflammatory indications, competing in the same physician-prescribed biologic asthma space that rademikibart targets with its anti-IL-4Rα approach.
  • GSK (GlaxoSmithKline): Markets Nucala (mepolizumab) and Trelegy in asthma and COPD, and has a substantial respiratory biologic franchise overlapping with rademikibart's lead indications. Directly comparable as an established respiratory immunology competitor.
  • Regeneron Pharmaceuticals: Co-developer of Dupixent (dupilumab), the leading IL-4Rα antibody and the direct therapeutic competitor to rademikibart in asthma, COPD, and atopic dermatitis. Most directly comparable peer given identical mechanism and overlapping indications.

Broad incumbents

  • Pfizer: Markets Cibinqo (abrocitinib) and Eucrisa in atopic dermatitis, as well as broader respiratory and inflammation assets. Comparable as a broad incumbent in the inflammatory dermatology and respiratory disease categories overlapping with rademikibart's indications.
  • Eli Lilly: Markets Olumiant (baricitinib, JAK inhibitor) and Taltz in inflammatory diseases including atopic dermatitis and asthma-adjacent indications. Comparable as a broad incumbent in the inflammatory disease space where rademikibart competes.

Emerging players

  • Arcutis Biotherapeutics: Commercial-stage dermatology company developing topical and biologic therapies for inflammatory skin diseases including atopic dermatitis. Comparable as an emerging immunology/dermatology player with overlapping addressable market, though smaller and focused on topicals.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Connect Biopharma social profiles

Digital presence

Connect Biopharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Connect Biopharma leadership team

Management profile

Number of profiles

Profiles2 records

Connect Biopharma funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Connect Biopharma 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 Connect Biopharma

What does Connect Biopharma do?

Connect Biopharma is a clinical-stage biopharmaceutical company developing rademikibart, a next-generation anti-IL-4Rα antibody designed to treat acute asthma and COPD exacerbations as well as atopic dermatitis. The company also has icanbelimod (CBP-307) in its pipeline for ulcerative colitis. It licenses rademikibart to Simcere Pharmaceutical for Greater China and is pre-revenue.

Is Connect Biopharma a public or private company?

Connect Biopharma is a public company. It is classified as public and is currently operating.

When was Connect Biopharma founded?

Connect Biopharma was founded in 2012. It employs 51 to 100 people.

Where is Connect Biopharma based?

Connect Biopharma is headquartered in San Diego, United States, in the North America region.

How does Connect Biopharma make money?

Two revenue lines are on record. Drug Development and Commercialization is the primary driver. The others are licensing Revenue - Simcere Partnership.

Who are Connect Biopharma's main competitors?

Direct peers on record are AstraZeneca, Sanofi, Galderma, Amgen, Novartis, GSK (GlaxoSmithKline) and Regeneron Pharmaceuticals. Broad incumbents are Pfizer and Eli Lilly. Arcutis Biotherapeutics is listed as an emerging player.

Does Connect Biopharma have an API?

No public API is recorded for Connect Biopharma.

What industry is Connect Biopharma in?

Connect Biopharma's product category is Biopharmaceuticals. Its primary akta.pro industry code is HLAIAAAH, Respiratory & Allergy Pharmaceuticals, with a secondary code of HLAIACAB, Immunology & Autoimmune Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2834.

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Live signals
The future of tradingConnect Biopharma says Phase 2 trial shows rademikibart cuts COPD treatment failure rate 81% through Week 4Connect Biopharma reported positive preliminary results from a global Phase 2 trial of rademikibart in acute COPD flare-ups, showing reduced treatment failures versus placebo. The drug also lowered new moderate-to-severe flare-ups, with no emergency visits or hospitalizations in the treatment arm. The company plans to seek FDA alignment on a Phase 3 registrational program.The future of tradingConnect Biopharma Announces Positive Preliminary Topline Data from its Global Phase 2 Study of Rademikibart as an Add-on Treatment for Acute Exacerbations in Adults with COPD and Type 2 InflammationConnect Biopharma announced positive preliminary topline data from its global Phase 2 study of rademikibart for acute exacerbations in COPD patients with type 2 inflammation. The study showed rademikibart reduced treatment failure by 81%, new moderate-to-severe exacerbations by 85%, and hospitalizations or ED visits by 100% through one month. The company plans to engage the FDA on a Phase 3 program.FierceBiotechConnect’s Dupixent rival reduces COPD attacks by 85%, but misses a secondary goalConnect Biopharma reported phase 2 data for rademikibart in COPD, showing an 81% reduction in treatment failure and an 85% reduction in moderate-to-severe exacerbations. The study missed a secondary FEV1 endpoint, but the company plans to propose it as an endpoint for a phase 3 trial.BioSpaceConnect Biopharma Announces Positive Preliminary Topline Data from its Global Phase 2 Study of Rademikibart as an Add-on Treatment for Acute Exacerbations in Adults with COPD and Type 2 InflammationConnect Biopharma announced topline results from its global Phase 2 study of rademikibart for acute COPD exacerbations, showing an 81% reduction in treatment failure and 85% fewer new moderate-to-severe exacerbations through one month. The drug also eliminated hospitalizations or ED visits for new exacerbations, and the company plans to engage the FDA on a Phase 3 program.AdvfnConnect Biopharma Rademikibart Phase 2 Data Shows Lung Function Improvement but Primary Endpoint Misses SignificanceConnect Biopharma reported Phase 2 data for rademikibart in acute asthma, showing a statistically significant 130 mL FEV1 improvement at Day 7 (p=0.023) but a non-significant 66% reduction in treatment failures (p=0.153). The company plans to seek FDA alignment on a Phase 3 program, with COPD trial data expected in September.Stock TitanConnect Biopharma to Present at H.C. Wainwright Sept. 15Connect Biopharma will host a fireside chat with management at the H.C. Wainwright 28th Annual Global Investment Conference on September 15, 2026, at 11:30 a.m. ET. The live webcast is available via the company's investor page, with a replay for about 90 days. The company is advancing rademikibart for asthma and COPD, with an exclusive license to Simcere in Greater China.Investing.comPiper Sandler initiates Connect Biopharma stock with overweight rating By Investing.comPiper Sandler initiated coverage on Connect Biopharma Holdings Ltd with an Overweight rating and a $7.00 price target, representing substantial upside from the current stock price of $2.07. The analyst highlighted rademikibart's potential as the only biologic in development for acute asthma and COPD exacerbations, with near-term catalysts including September 2026 Seabreeze STAT topline data in asthma. The firm estimates peak risk-adjusted acute sales of approximately $165 million and projects chronic sales of approximately $1.26 billion.Investing.comPiper Sandler initiates Connect Biopharma stock with overweight rating By Investing.comPiper Sandler initiated coverage on Connect Biopharma Holdings Ltd with an Overweight rating and a $7.00 price target, representing substantial upside from the current stock price of $2.07. The firm highlighted the drug candidate rademikibart's differentiated mechanism as potentially the only biologic in development for acute asthma and COPD exacerbations, estimating peak risk-adjusted acute sales of approximately $165 million and chronic sales of approximately $1.26 billion. Connect Biopharma has completed enrollment in its Phase 2 Seabreeze STAT Asthma study with 160 global participants, with topline data expected in early September 2026.Investing.comH.C. Wainwright reiterates Buy on Connect Biopharma stock at $7 By Investing.comH.C. Wainwright reiterated a Buy rating on Connect Biopharma Holdings Ltd with a $7.00 price target, representing 230% upside from the current stock price of $2.12. Connect Biopharma has completed enrollment in its Phase 2 Seabreeze STAT Asthma study evaluating rademikibart for acute exacerbations in asthma patients, with 160 participants enrolled globally and topline data expected in early September 2026.Investing.comConnect Biopharma stock rises after Phase 2 asthma study enrollment By Investing.comConnect Biopharma Holdings Ltd announced completion of enrollment in its Phase 2 Seabreeze STAT Asthma study evaluating rademikibart for acute exacerbations in asthma patients with type 2 inflammation. The company's shares rose 8% following the announcement, with topline data expected in early September 2026. Connect Biopharma also plans to complete enrollment in its Seabreeze STAT COPD study this month and meet with the FDA later this year to align on a Phase 3 program.