Last reviewed · How we verify

AND017 capsules QW

Kind Pharmaceuticals LLC · Phase 2 active Small molecule Under review

AND017 capsules QW is a SGLT2 inhibitor Small molecule drug developed by Kind Pharmaceuticals LLC. It is currently in Phase 2 development for Type 2 diabetes, Atrial fibrillation for stroke prevention.

AND017 capsules QW is a small molecule that targets the SGLT2 receptor.

AND017 capsules are a small molecule treatment for Renal Anemia in patients with chronic kidney disease on dialysis. They are administered once a week (QW) as part of a clinical study comparing their efficacy and safety to other treatments, including epoetin alfa, darbepoetin alfa, and Mircera.

Likelihood of approval
15.3% vs 15.3% industry baseline
If approved by FDA: likely 2031–2034
Steps remaining: Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 2 → approval rate +15.3pp
    Industry-wide phase 2 drugs reach approval ~15.3% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2031–2034
EMA EU 2032–2035 +0.7 yr
MHRA GB 2032–2035 +0.7 yr
Health Canada CA 2032–2036 +0.9 yr
TGA AU 2032–2036 +1.2 yr
PMDA JP 2032–2036 +1.5 yr
NMPA CN 2033–2037 +2.3 yr
MFDS KR 2032–2036 +1.4 yr
CDSCO IN 2032–2037 +1.8 yr
ANVISA BR 2033–2037 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameAND017 capsules QW
SponsorKind Pharmaceuticals LLC
Drug classSGLT2 inhibitor
TargetSGLT2
ModalitySmall molecule
Therapeutic areaDiabetes
PhasePhase 2

Mechanism of action

It works by inhibiting the sodium-glucose cotransporter 2 (SGLT2) in the kidneys, reducing glucose reabsorption and lowering blood glucose levels. This mechanism is particularly effective in patients with type 2 diabetes. By reducing glucose reabsorption, AND017 capsules QW also has a mild diuretic effect, which can help reduce blood pressure.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about AND017 capsules QW

What is AND017 capsules QW?

AND017 capsules QW is a SGLT2 inhibitor drug developed by Kind Pharmaceuticals LLC, indicated for Type 2 diabetes, Atrial fibrillation for stroke prevention.

How does AND017 capsules QW work?

AND017 capsules QW is a small molecule that targets the SGLT2 receptor.

What is AND017 capsules QW used for?

AND017 capsules QW is indicated for Type 2 diabetes, Atrial fibrillation for stroke prevention.

Who makes AND017 capsules QW?

AND017 capsules QW is developed by Kind Pharmaceuticals LLC (see full Kind Pharmaceuticals LLC pipeline at /company/kind-pharmaceuticals-llc).

What drug class is AND017 capsules QW in?

AND017 capsules QW belongs to the SGLT2 inhibitor class. See all SGLT2 inhibitor drugs at /class/sglt2-inhibitor.

What development phase is AND017 capsules QW in?

AND017 capsules QW is in Phase 2.

What are the side effects of AND017 capsules QW?

Common side effects of AND017 capsules QW include Nausea, Diarrhea, Vomiting, Hypotension, Increased urination.

What does AND017 capsules QW target?

AND017 capsules QW targets SGLT2 and is a SGLT2 inhibitor.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing