R1 Therapeutics
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.
- Company typePrivate
- Founded2026
- HeadquartersLondon, United Kingdom
- Headcount1–10
- GTM typeB2B
- OfferingHardware or Manufacturing
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
Where R1 Therapeutics is headquartered
LocationHeadquarters
- 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
- 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.
- 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
| Model | Billing | Price |
|---|---|---|
| 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 offeringCore 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 profileSegments3 records
Ideal customer profiles2 records
R1 Therapeutics technology and API
TechnologyTechnology 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 signalScale indicators7 records
Recent moves5 records
Expansion highlights6 records
R1 Therapeutics competitors and assessment
Company assessmentEmerging 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 presenceR1 Therapeutics compliance and trust
Trust signalCompliance1 record
R1 Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
R1 Therapeutics leadership team
Management profileNumber of profiles
Profiles8 records
R1 Therapeutics subsidiaries and ownership
Company hierarchySubsidiaries1 record
R1 Therapeutics funding detail
Funding detailFunding 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 investmentM&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.