Developer docs
API playgroundTry for free, no card

Search company profiles

R1 Therapeutics

Full company profile

uuid00vqk9f

Namestring
R1 Therapeutics
Legal namestring
R1 Therapeutics, Inc.
Company typeenum
Private
Founded yearint
2026
Descriptiontext

R1 Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class oral therapies for kidney disease, with a lead asset, AP306, in development as a monotherapy for hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. The company launched in March 2026 alongside an oversubscribed $77.5 million Series A financing co-led by Abingworth, DaVita Venture Group, and F-Prime, with participation from Curie.Bio, SymBiosis, and U.S. Renal Care. R1 is headquartered in Redwood City/San Francisco, California, with additional offices in San Diego and Raleigh, North Carolina, and a UK affiliate (R1 Therapeutics Ltd) registered in London. Its co-founders are CEO Krishna Polu, M.D. (a practicing nephrologist with 20+ years of biopharmaceutical experience) and COO L. Mary Smith, Ph.D. (former Chief Development Officer at SpringWorks Therapeutics).

AP306 (previously known as EOS789, originally discovered by Chugai Pharmaceutical) is a first-in-class pan phosphate transporter inhibitor — a small molecule that uniquely blocks the active transport of phosphate in the gastrointestinal tract by inhibiting three sodium-dependent phosphate transporters (NaPi-IIb, PiT-1, PiT-2), a mechanism distinct from the passive-binding phosphate binders that have constituted standard of care for approximately 60 years. In a Phase 2a study in dialysis patients, AP306 achieved -2.51 mg/dL serum phosphorus reduction (95% CI -3.07, -1.92) at an average 98.0 mg TID dose, compared with -1.08 mg/dL (95% CI -1.58, -0.59) for Sevelamer at 1,571.4 mg TID. R1 holds exclusive global development and commercialization rights to AP306 outside Greater China via an in-license from Alebund Pharmaceuticals, with a joint global Phase 2b multi-regional trial in the U.S. and China planned to start later in 2026; Alebund retains rights within Greater China. The company is currently pre-revenue; future revenue is expected to come from commercialization of AP306 (specialist field sales to nephrologists and dialysis providers, leveraging the DaVita and U.S. Renal Care networks) supplemented by milestone payments and tiered royalties from Alebund.

Short descriptiontext

R1 Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class oral therapies for kidney disease. Its lead asset, AP306, is a pan phosphate transporter inhibitor for hyperphosphatemia in chronic kidney disease patients on dialysis. Pre-revenue; raised $77.5M Series A in March 2026.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersLondon, United Kingdom
HQ citystring
London
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices5 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
renal therapeutics, phosphate transporter inhibition, chronic kidney disease drugs, hyperphosphatemia treatment, clinical-stage biopharmaceuticals
Industry2 codes
1Rare Renal & Nephrology Disorder Therapies
CodeHLAIAIAIPrimaryYes
2Real-World Evidence (RWE) & HEOR for Development
CodeHLAIALAIPrimaryNo
NAICS code2 codes
  • Scientific Research and Development Services5417
  • Pharmaceutical and Medicine Manufacturing3254
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Nephrology Pharmaceuticals (Chronic Kidney Disease Therapeutics)
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Future drug commercialization (pre-revenue)
TypeHardware Sales
Description

R1 Therapeutics is a clinical-stage biopharmaceutical company and is currently pre-revenue. Future revenue expected from commercialization of AP306 as a monotherapy for hyperphosphatemia in CKD patients on dialysis, leveraging exclusive global development and commercial rights outside Greater China licensed from Alebund Pharmaceuticals.

r1therapeutics.com
2Licensing royalties and milestone payments (out-license to Alebund for Greater China)
TypeLicensing Royalties
Description

R1 holds exclusive rights outside Greater China; Alebund retains rights within Greater China. Alebund agreement includes potential milestone payments of up to low triple-digit millions of U.S. dollars and tiered royalties in low double-digit percentages on sales.

en.prnasia.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
Pricing details1 tier
1Not publicly disclosed — clinical-stage asset in development
ModelOther
Notes

AP306 is in Phase 2b development (entering Phase 2b later in 2026). No commercial pricing exists yet. Once approved, it would likely be priced as a prescription pharmaceutical for chronic outpatient use in dialysis patients.

r1therapeutics.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

R1 Therapeutics is a clinical-stage biopharmaceutical company developing AP306, a first-in-class, oral, small-molecule pan phosphate transporter inhibitor being advanced as a monotherapy for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. The company holds exclusive global development and commercialization rights for AP306 outside of Greater China under a license from Alebund Pharmaceuticals, with global Phase 2b clinical development planned to commence later in 2026.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • Phase 2a: AP306 reduced serum phosphorus by -2.51 mg/dL from baseline (95% CI -3.07, -1.92) vs Sevelamer -1.08 mg/dL (95% CI -1.58, -0.59) over 12 weeks in dialysis patients.
+5 more records
Product overview1 text field

R1 Therapeutics operates a single-asset-focused clinical-stage biopharmaceutical portfolio centered on its lead program AP306, rather than a platform-plus-modules product architecture. The company's offering is built around AP306, a first-in-class pan phosphate transporter inhibitor being advanced as a monotherapy for hyperphosphatemia in chronic kidney disease (CKD) patients on dialysis, with global development and commercialization rights (outside Greater China) licensed from Alebund Pharmaceuticals. AP306 constitutes the entirety of R1's disclosed pipeline, and the company's broader product scope is envisioned to extend over time across the spectrum of kidney disease, including CKD non-dialysis populations, dialysis, and kidney transplant, though no additional named clinical assets have been disclosed.

Product and service1 record
1AP306
CategoryLead clinical-stage drug candidate / Nephrology pharmaceutical (hyperphosphatemia)
Description

AP306 is a first-in-class, oral, small-molecule pan phosphate transporter inhibitor in development as a monotherapy for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. It is the only agent that blocks the active transport of phosphate by targeting three key sodium-dependent phosphate transporters in the gastrointestinal tract (NaPi-IIb, PiT-1, PiT-2), offering the potential for superior efficacy with a substantially lower pill burden compared to existing phosphate binder therapies.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

ProKidney is a clinical-stage cell-therapy company developing rilparencel for CKD. While operating in a different modality, it is an emerging player in the same target market (CKD) and a comparable clinical-stage, indication-focused biotech pursuing a high-conviction thesis in kidney disease.

TypeDirect peer
Description

Travere commercializes FILSPARI (sparsentan) for IgA nephropathy and is developing additional CKD assets. It is a directly comparable late-stage nephrology-focused biopharma targeting a CKD subpopulation, sharing the model of bringing novel small molecules to underserved renal indications.

TypeBroad incumbent
Description

Chinook was a clinical-stage nephrology company (acquired by Novartis in 2023) developing atrasentan for IgA nephropathy and other CKD assets. It represents the most relevant 'acquired-and-scaled' comparable for a kidney-focused clinical-stage biotech, now operating within a large pharma.

TypeOthers
Description

Chugai originally discovered AP306 (as EOS789) before licensing it to Alebund. As a large Japanese biopharma with a major renal and CKD franchise, it is an enabling/thematic comparable in nephrology drug development but not a direct competitor to R1.

TypeDirect peer
Description

Ardelyx developed and commercializes XPHOZAH (tenapanor), the only FDA-approved non-binder therapy for hyperphosphatemia in CKD patients on dialysis. It is the most directly comparable company to R1 Therapeutics as the only other approved or late-stage asset specifically targeting phosphate control in dialysis via a novel mechanism.

TypeEmerging player
Description

Cara developed KORSUVA (difelikefalin) for chronic kidney disease-associated pruritus, addressing a major comorbidity in dialysis patients. It is an emerging peer in the dialysis-adjacent specialty and a useful comparable for nephrology-focused commercial launches.

TypeBroad incumbent
Description

Akebia developed and commercializes AURYXIA (ferric citrate) for hyperphosphatemia in CKD dialysis patients and vadadustat for anemia. It is a broad incumbent in the renal space and a direct competitor in the hyperphosphatemia market AP306 targets.

TypeBroad incumbent
Description

Otsuka markets JYNARQUE (tolvaptan) for autosomal dominant polycystic kidney disease, the only FDA-approved therapy to slow ADPKD progression. It is a broad incumbent with a commercialized renal franchise, providing a reference for the scale and infrastructure needed to commercialize in nephrology.

TypeDirect peer
Description

Vera is a clinical-stage nephrology company developing atacicept for IgA nephropathy. It is a directly comparable late-stage, indication-focused kidney biotech with similar funding, single-asset lead, and clinical-development profile.

TypeOthers
Description

Alebund is R1's exclusive licensor for AP306 ex-Greater China and holds the Greater China rights. It is an enabling partner with a parallel in-house renal franchise and is a direct comparable as an Asia-rooted clinical-stage nephrology company, but not a competitive peer.

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 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 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
Profiles8 records

Each record includes

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

Subsidiaries1 record

Each record includes

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

Compliance1 record

Each record includes

Name, Class, Description

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

Investors6 records

Each record includes

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

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

M&A

Each record includes

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

Investment

Each record includes

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

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

R1 Therapeutics

Nephrology Pharmaceuticals (Chronic Kidney Disease Therapeutics)r1therapeutics.com

R1 Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class oral therapies for kidney disease. Its lead asset, AP306, is a pan phosphate transporter inhibitor for hyperphosphatemia in chronic kidney disease patients on dialysis. Pre-revenue; raised $77.5M Series A in March 2026.

What R1 Therapeutics does

R1 Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class oral therapies for kidney disease, with a lead asset, AP306, in development as a monotherapy for hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. The company launched in March 2026 alongside an oversubscribed $77.5 million Series A financing co-led by Abingworth, DaVita Venture Group, and F-Prime, with participation from Curie.Bio, SymBiosis, and U.S. Renal Care. R1 is headquartered in Redwood City/San Francisco, California, with additional offices in San Diego and Raleigh, North Carolina, and a UK affiliate (R1 Therapeutics Ltd) registered in London. Its co-founders are CEO Krishna Polu, M.D. (a practicing nephrologist with 20+ years of biopharmaceutical experience) and COO L. Mary Smith, Ph.D. (former Chief Development Officer at SpringWorks Therapeutics).

AP306 (previously known as EOS789, originally discovered by Chugai Pharmaceutical) is a first-in-class pan phosphate transporter inhibitor — a small molecule that uniquely blocks the active transport of phosphate in the gastrointestinal tract by inhibiting three sodium-dependent phosphate transporters (NaPi-IIb, PiT-1, PiT-2), a mechanism distinct from the passive-binding phosphate binders that have constituted standard of care for approximately 60 years. In a Phase 2a study in dialysis patients, AP306 achieved -2.51 mg/dL serum phosphorus reduction (95% CI -3.07, -1.92) at an average 98.0 mg TID dose, compared with -1.08 mg/dL (95% CI -1.58, -0.59) for Sevelamer at 1,571.4 mg TID. R1 holds exclusive global development and commercialization rights to AP306 outside Greater China via an in-license from Alebund Pharmaceuticals, with a joint global Phase 2b multi-regional trial in the U.S. and China planned to start later in 2026; Alebund retains rights within Greater China. The company is currently pre-revenue; future revenue is expected to come from commercialization of AP306 (specialist field sales to nephrologists and dialysis providers, leveraging the DaVita and U.S. Renal Care networks) supplemented by milestone payments and tiered royalties from Alebund.

R1 Therapeutics firmographics

Firmographics
Name
R1 Therapeutics
Legal name
R1 Therapeutics, Inc.
Website
https://r1therapeutics.com
Company type
Private
Founded year
2026
Operating status
Operating
Headcount range
1–10 employees
Short description
R1 Therapeutics is a clinical-stage biopharmaceutical company developing first-in-class oral therapies for kidney disease. Its lead asset, AP306, is a pan phosphate transporter inhibitor for hyperphosphatemia in chronic kidney disease patients on dialysis. Pre-revenue; raised $77.5M Series A in March 2026.
Ownership category
akta.pro rank

R1 Therapeutics industry classification

Industry
Product category
Nephrology Pharmaceuticals (Chronic Kidney Disease Therapeutics)
NAICS
Scientific Research and Development Services (5417), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Rare Renal & Nephrology Disorder Therapies (HLAIAIAI)
akta.pro secondary industry
Real-World Evidence (RWE) & HEOR for Development (HLAIALAI)

Keywords

  • Renal therapeutics
  • Phosphate transporter inhibition
  • Chronic kidney disease drugs
  • Hyperphosphatemia treatment
  • Clinical-stage biopharmaceuticals

Where R1 Therapeutics is headquartered

Location

Headquarters

HQ city
London
HQ country
United Kingdom
HQ region
Europe

Offices5 records

Markets served

R1 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. Future drug commercialization (pre-revenue): R1 Therapeutics is a clinical-stage biopharmaceutical company and is currently pre-revenue. Future revenue expected from commercialization of AP306 as a monotherapy for hyperphosphatemia in CKD patients on dialysis, leveraging exclusive global development and commercial rights outside Greater China licensed from Alebund Pharmaceuticals.
  2. Licensing royalties and milestone payments (out-license to Alebund for Greater China): R1 holds exclusive rights outside Greater China; Alebund retains rights within Greater China. Alebund agreement includes potential milestone payments of up to low triple-digit millions of U.S. dollars and tiered royalties in low double-digit percentages on sales.

Pricing tiers

ModelBillingPrice
Other—Not publicly disclosed — clinical-stage asset in development

Go-to-market motion2 records

Distribution channels2 records

Marketing channels7 records

R1 Therapeutics product offering

Product offering

Core offering

R1 Therapeutics is a clinical-stage biopharmaceutical company developing AP306, a first-in-class, oral, small-molecule pan phosphate transporter inhibitor being advanced as a monotherapy for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. The company holds exclusive global development and commercialization rights for AP306 outside of Greater China under a license from Alebund Pharmaceuticals, with global Phase 2b clinical development planned to commence later in 2026.

Product overview

R1 Therapeutics operates a single-asset-focused clinical-stage biopharmaceutical portfolio centered on its lead program AP306, rather than a platform-plus-modules product architecture. The company's offering is built around AP306, a first-in-class pan phosphate transporter inhibitor being advanced as a monotherapy for hyperphosphatemia in chronic kidney disease (CKD) patients on dialysis, with global development and commercialization rights (outside Greater China) licensed from Alebund Pharmaceuticals. AP306 constitutes the entirety of R1's disclosed pipeline, and the company's broader product scope is envisioned to extend over time across the spectrum of kidney disease, including CKD non-dialysis populations, dialysis, and kidney transplant, though no additional named clinical assets have been disclosed.

Differentiator

Problem solved

Functional benefit

Products and services

  • AP306 AP306 is a first-in-class, oral, small-molecule pan phosphate transporter inhibitor in development as a monotherapy for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. It is the only agent that blocks the active transport of phosphate by targeting three key sodium-dependent phosphate transporters in the gastrointestinal tract (NaPi-IIb, PiT-1, PiT-2), offering the potential for superior efficacy with a substantially lower pill burden compared to existing phosphate binder therapies.

Quantifiable outcome

  • Phase 2a: AP306 reduced serum phosphorus by -2.51 mg/dL from baseline (95% CI -3.07, -1.92) vs Sevelamer -1.08 mg/dL (95% CI -1.58, -0.59) over 12 weeks in dialysis patients.
  • +5 more outcomes

Companies that use R1 Therapeutics

Customer profile

Segments3 records

Ideal customer profiles2 records

R1 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

R1 Therapeutics partnerships and signals

Strategic signal

Scale indicators7 records

Recent moves5 records

Expansion highlights6 records

R1 Therapeutics competitors and assessment

Company assessment

Emerging players

  • ProKidney: ProKidney is a clinical-stage cell-therapy company developing rilparencel for CKD. While operating in a different modality, it is an emerging player in the same target market (CKD) and a comparable clinical-stage, indication-focused biotech pursuing a high-conviction thesis in kidney disease.
  • Cara Therapeutics: Cara developed KORSUVA (difelikefalin) for chronic kidney disease-associated pruritus, addressing a major comorbidity in dialysis patients. It is an emerging peer in the dialysis-adjacent specialty and a useful comparable for nephrology-focused commercial launches.

Direct peers

  • Travere Therapeutics: Travere commercializes FILSPARI (sparsentan) for IgA nephropathy and is developing additional CKD assets. It is a directly comparable late-stage nephrology-focused biopharma targeting a CKD subpopulation, sharing the model of bringing novel small molecules to underserved renal indications.
  • Ardelyx: Ardelyx developed and commercializes XPHOZAH (tenapanor), the only FDA-approved non-binder therapy for hyperphosphatemia in CKD patients on dialysis. It is the most directly comparable company to R1 Therapeutics as the only other approved or late-stage asset specifically targeting phosphate control in dialysis via a novel mechanism.
  • Vera Therapeutics: Vera is a clinical-stage nephrology company developing atacicept for IgA nephropathy. It is a directly comparable late-stage, indication-focused kidney biotech with similar funding, single-asset lead, and clinical-development profile.

Broad incumbents

  • Chinook Therapeutics (a Novartis company): Chinook was a clinical-stage nephrology company (acquired by Novartis in 2023) developing atrasentan for IgA nephropathy and other CKD assets. It represents the most relevant 'acquired-and-scaled' comparable for a kidney-focused clinical-stage biotech, now operating within a large pharma.
  • Akebia Therapeutics: Akebia developed and commercializes AURYXIA (ferric citrate) for hyperphosphatemia in CKD dialysis patients and vadadustat for anemia. It is a broad incumbent in the renal space and a direct competitor in the hyperphosphatemia market AP306 targets.
  • Otsuka Pharmaceutical: Otsuka markets JYNARQUE (tolvaptan) for autosomal dominant polycystic kidney disease, the only FDA-approved therapy to slow ADPKD progression. It is a broad incumbent with a commercialized renal franchise, providing a reference for the scale and infrastructure needed to commercialize in nephrology.

Others

  • Chugai Pharmaceutical: Chugai originally discovered AP306 (as EOS789) before licensing it to Alebund. As a large Japanese biopharma with a major renal and CKD franchise, it is an enabling/thematic comparable in nephrology drug development but not a direct competitor to R1.
  • Alebund Pharmaceuticals: Alebund is R1's exclusive licensor for AP306 ex-Greater China and holds the Greater China rights. It is an enabling partner with a parallel in-house renal franchise and is a direct comparable as an Asia-rooted clinical-stage nephrology company, but not a competitive peer.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

R1 Therapeutics social profiles

Digital presence

R1 Therapeutics compliance and trust

Trust signal

Compliance1 record

R1 Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

R1 Therapeutics leadership team

Management profile

Number of profiles

Profiles8 records

R1 Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

R1 Therapeutics funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors6 records

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

R1 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 R1 Therapeutics

What does R1 Therapeutics do?

R1 Therapeutics is a clinical-stage biopharmaceutical company developing AP306, a first-in-class, oral, small-molecule pan phosphate transporter inhibitor being advanced as a monotherapy for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD) on dialysis. The company holds exclusive global development and commercialization rights for AP306 outside of Greater China under a license from Alebund Pharmaceuticals, with global Phase 2b clinical development planned to commence later in 2026.

Is R1 Therapeutics a public or private company?

R1 Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was R1 Therapeutics founded?

R1 Therapeutics was founded in 2026. It employs 1 to 10 people.

Where is R1 Therapeutics based?

R1 Therapeutics is headquartered in London, United Kingdom, in the Europe region.

How does R1 Therapeutics make money?

Two revenue lines are on record. Future drug commercialization (pre-revenue) is the primary driver. The others are licensing royalties and milestone payments (out-license to Alebund for Greater China).

Who are R1 Therapeutics's main competitors?

Emerging players on record are ProKidney and Cara Therapeutics. Direct peers are Travere Therapeutics, Ardelyx and Vera Therapeutics. Broad incumbents are Chinook Therapeutics (a Novartis company), Akebia Therapeutics and Otsuka Pharmaceutical. Others are Chugai Pharmaceutical and Alebund Pharmaceuticals.

Does R1 Therapeutics have an API?

No public API is recorded for R1 Therapeutics.

What industry is R1 Therapeutics in?

R1 Therapeutics's product category is Nephrology Pharmaceuticals (Chronic Kidney Disease Therapeutics). Its primary akta.pro industry code is HLAIAIAI, Rare Renal & Nephrology Disorder Therapies, with a secondary code of HLAIALAI, Real-World Evidence (RWE) & HEOR for Development. Its NAICS code is 5417 and its SIC code is 8731.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
Clinical Trials ArenaR1 Therapeutics secures $80.5m to fund Phase IIb AP306 studyR1 Therapeutics expanded its Series A financing to $80.5m to advance AP306 in a Phase IIb trial for hyperphosphatemia in dialysis-dependent chronic kidney disease patients. The round includes Samsara BioCapital and expects top-line results in the first half of 2027.Pulse 2.0R1 Therapeutics Expands Series A To $80.5 Million To Advance AP306R1 Therapeutics expanded its Series A financing to $80.5 million, adding Samsara BioCapital to an existing syndicate. The funds support development of AP306, a phosphate transporter inhibitor for hyperphosphatemia in dialysis patients, with Phase 2b topline results expected in the first half of 2027.VC News DailyR1 Therapeutics Inks $80.5M Series A ExpansionR1 Therapeutics expanded its Series A financing to $80.5 million, adding Samsara BioCapital to the investor syndicate. The round follows an oversubscribed $77.5 million round announced in March 2026.PR Newswire APACAlebund Pharmaceuticals Announces 2026 Interim ResultsAlebund Pharmaceuticals reported first-half 2026 revenue of RMB104.2 million, up 761.2% year-on-year, with a net loss of RMB162.6 million, down 22.5%. The company completed patient enrollment in its AP301 Phase III trial and initiated the AP306 Phase IIb trial, with licensing revenue of RMB79.3 million from R1.PR NewswireHyperphosphatemia Market Set for Robust Growth During the Forecast Period (2026-2036), Driven by Novel Therapeutics and Rising CKD Burden | DelveInsightThe hyperphosphatemia market is projected to grow through 2036, driven by rising chronic kidney disease and dialysis populations. Prevalence reaches 2.3% in CKD stages III–IV, and emerging therapies like TS-172 and AP-301 are expected to reshape treatment. The US led the 7MM in 2025.PharmaTimesR1 Therapeutics begins global phase 2b trial of AP306 for hyperphosphatemiaR1 Therapeutics randomized the first patient in its global phase 2b trial of AP306, a pan phosphate transporter inhibitor for hyperphosphatemia in dialysis patients. The trial assesses safety, tolerability, and serum phosphate lowering across six fixed-dose regimens over eight weeks, with about 168 patients enrolled at US and China sites. Topline results are expected in the first half of 2027.PR NewswireAlebund Pharmaceuticals Announces First Participant Randomized and Dosed in Global Phase IIb Multi-Regional Clinical Trial of AP306 for HyperphosphatemiaAlebund Pharmaceuticals announced the first participant randomized and dosed in its global Phase IIb trial of AP306 for hyperphosphatemia in dialysis patients. The trial, co-sponsored with R1 Therapeutics, plans to enroll about 168 participants across six fixed-dose regimens or placebo over eight weeks, with topline results expected in the first half of 2027.PharmaTimesR1 Therapeutics forms advisory board to support advancement of AP306R1 Therapeutics formed a seven-member scientific advisory board to support AP306's advancement into global phase 2b trials for hyperphosphatemia in chronic kidney disease. The board is chaired by Glenn Chertow, and the appointments provide external validation of the company's scientific approach.GlobeNewswireR1 Therapeutics establishes world-class Scientific Advisory Board to support advancement of AP306 in Chronic Kidney DiseaseR1 Therapeutics announced its Scientific Advisory Board, chaired by Glenn Chertow, with seven nephrology experts. The board supports AP306, a pan phosphate transporter inhibitor, as it advances into global Phase 2b trials for hyperphosphatemia in chronic kidney disease. The company launched in March 2026 with a $77.5 million Series A.pharmaphorumKidney biotech R1's $78m debut, and other biofinancingsMarch has seen a cluster of biotech financing rounds, with six companies raising between $40 million and $78 million for candidates spanning chronic kidney disease, cancer cell therapies, and autoimmune diseases. R1 Therapeutics emerged from stealth with a $77.5 million Series A for a pan-phosphate transporter inhibitor (AP306) licensed from China's Alebund Pharmaceuticals, Crossbow Therapeutics raised $77 million for T-cell engagers targeting myeloid cancers, and Excalipoint Therapeutics secured $68.7 million for a trispecific cancer antibody. Additional rounds included Prolium Bioscience's $50 million Series A for an autoimmune TCE, Unnatural Products' $45 million Series B for macrocyclic peptide development, Vima Therapeutics' expansion to $100 million Series A for a movement disorder candidate, and Mestag Therapeutics' $40 million for a bispecific antibody heading to Phase 1 trials.