Dasatinib

BCR-ABL tyrosine kinase inhibitors · given by oral · on the market since 2006

Leads

44.7M

People

Makers

How abandoned

What it's made of

Each functional group on the molecule does a specific, predictable job.

SETS WHERE IT GOES

Basic amine

What it does. Neutral enough to slip through membranes, then becomes charged inside the acidic compartments of the cell and gets trapped there. Concentrations inside cells can reach many times the blood level.

What it opens up. Diseases of the cell's internal recycling compartments, and a common reason a drug accumulates in lung, liver, and eye tissue far beyond what the blood level suggests.

SETS HOW LONG IT LASTS

Aromatic halogen

What it does. Slows liver breakdown and increases membrane crossing. Also fills space in a binding pocket, which often raises potency several-fold.

What it opens up. Better tissue penetration and longer duration, at the cost of higher fat storage.

Where it can get to

Predicted from molecular weight, lipophilicity, polar surface area and hydrogen-bond donor count. A drug can only act where it distributes, so this constrains which conditions are addressable before any biology is considered. derived

Easily

Systemic circulation

Absorbed from the gut and distributed in plasma.

Barely

Central nervous system

Crosses the blood–brain barrier.

Intestinal lumen only

Poorly absorbed. Acts locally in the gut with minimal systemic exposure.

Partly

Skin

Crosses the stratum corneum. Viable as a topical.

Barely

Urinary tract

Cleared unchanged in urine. Local concentration exceeds plasma.

What it binds — and whether we can reach it · 8 of 7 reachable

Binding affinity is only meaningful against the plasma concentration reached at the approved dose. A target requiring higher concentrations cannot be engaged in a patient, whatever the in vitro potency. Most repurposing hypotheses fail at this step, and it is rarely checked before a trial is proposed. measured

Values are pAct — the negative logarithm of the molar concentration at which the drug half-occupies the target. Each whole step is a tenfold difference in potency: 9.0 = 1 nanomolar, 6.0 = 1 micromolar, 5.0 = 10 micromolar. Oral drugs typically reach 0.1–10 micromolar in plasma, so roughly 6.0 is the threshold below which a target cannot be reached at a tolerated dose. Figures come from DrugCentral’s curated binding data.

LCK

Kinase · inhibitor

9.7

Engaged easily

SRC

Kinase · inhibitor

9.68

Engaged easily

ABL1

Kinase · inhibitor

9.6

Engaged easily

YES1

Kinase · inhibitor

9.52

Engaged easily

KIT

Kinase · inhibitor

9.24

Engaged easily

PDGFRB

Kinase · inhibitor

9.2

Engaged easily

FYN

Kinase · inhibitor

9.1

Engaged easily

Target	Kind	Action	Affinity (pAct)	Can it be engaged?
LCK	Kinase	inhibitor	9.7	Engaged easily
SRC	Kinase	inhibitor	9.68	Engaged easily
ABL1	Kinase	inhibitor	9.6	Engaged easily
YES1	Kinase	inhibitor	9.52	Engaged easily
KIT	Kinase	inhibitor	9.24	Engaged easily
PDGFRB	Kinase	inhibitor	9.2	Engaged easily
FYN	Kinase	inhibitor	9.1	Engaged easily

This molecule builds up inside cells far above blood levels. Local concentration therefore exceeds plasma, so targets that look unreachable on a plasma reading may still be engaged. assumed

New uses, and who is already trying them

One card per candidate indication: the reasoning link by link, the evidence tier that governs how strongly it can be stated, and any registered trials.

5 of the 142 conditions linked to this drug’s targets have been checked against trial records so far. The rest are not ruled out — they are unchecked.

3 possible uses were rejected for pushing the wrong way. The target is linked to the condition, but the drug modulates it in the wrong direction.

Not yet used for these — 5

gastrointestinal stromal tumor

Tried in people

It showed an effect in a human trial that was not followed up.

The condition

Gastrointestinal stromal tumor (GIST) is the most common mesenchymal neoplasm of the gastrointestinal (GI) tract, typically presenting in adults over the age of 40 (mean age 63), and only rarely in children, in various regions of the GI tract, most commonly the stomach or small intestine but also less commonly in the esophagus, appendix, rectum and colon. GISTs can be asymptomatic or present with various non-specific signs, depending on the location and size of tumor, such as loss of appetite, anemia, weight loss,

KIT · KIT proto-oncogene, receptor tyrosine kinase

Tyrosine-protein kinase that acts as a cell-surface receptor for the cytokine KITLG/SCF and plays an essential role in the regulation of cell survival and proliferation, hematopoiesis, stem cell maintenance, gametogenesis, mast cell development, migration and function, and in melanogenesis. In response to KITLG/SCF binding, KIT can activate several signaling pathways. Phosphorylates PIK3R1, PLCG1, SH2B2/APS and CBL. Activates the AKT1 signaling pathway by phosphorylation of PIK3R1, the regulatory subunit of phospha

Open Targets scores each kind of evidence from 0.00 to 1.00 for this exact pairing — KIT and gastrointestinal stromal tumor. The score reflects how much evidence of that kind exists and how consistent it is. It is not a probability that the drug works. Rows are ordered by how much each kind counts toward the evidence figure used in the ranking, not by its raw score, because the two disagree: literature co-occurrence saturates near 1.00 on almost any well-studied pair, while genetic association rarely exceeds 0.70 even when causal.

Genetic association0.91 / 1.00

Inherited variants in this gene alter disease risk in human populations. The datatype most predictive of later clinical success.55% of evidence score

Somatic mutation0.78 / 1.00

This gene is recurrently mutated in this tumour type.15% of evidence score

Animal model0.48 / 1.00

Altering this gene in animals reproduces or relieves the disease phenotype.15% of evidence score

Pathway0.90 / 1.00

The gene sits in a pathway with established disruption in this condition.8% of evidence score

Curated genetic literature0.82 / 1.00

Gene–disease links curated from published genetic studies.5% of evidence score

Literature co-occurrence0.99 / 1.00

Gene and condition appear together in published text. Reflects publication volume, not causal evidence.2% of evidence score

Clinical0.98 / 1.00

Derived from clinical or trial records.not counted

Phase 3 has run

A Phase 3 trial exists. Read its result before anything else.

NCT00688766 Study Evaluating IPI-504 in Patients Wit · Ph 3 · 47 people

+6 more on ClinicalTrials.gov

What would kill it. A null result in the completed Phase 3.

chronic myelogenous leukemia, BCR-ABL1 positive

Tried in people

It showed an effect in a human trial that was not followed up.

The condition

A chronic myeloproliferative neoplasm characterized by the expression of the BCR-ABL1 fusion gene. It presents with neutrophilic leukocytosis. It can appear at any age, but it mostly affects middle aged and older individuals. Patients usually present with fatigue, weight loss, anemia, night sweats, and splenomegaly. If untreated, it follows a biphasic or triphasic natural course; an initial indolent chronic phase which is followed by an accelerated phase, a blast phase, or both. Allogeneic stem cell transplantation

ABL1 · ABL proto-oncogene 1, non-receptor tyrosine kinase

Non-receptor tyrosine-protein kinase that plays a role in many key processes linked to cell growth and survival such as cytoskeleton remodeling in response to extracellular stimuli, cell motility and adhesion, receptor endocytosis, autophagy, DNA damage response and apoptosis. Coordinates actin remodeling through tyrosine phosphorylation of proteins controlling cytoskeleton dynamics like WASF3 (involved in branch formation); ANXA1 (involved in membrane anchoring); DBN1, DBNL, CTTN, RAPH1 and ENAH (involved in signa

Open Targets scores each kind of evidence from 0.00 to 1.00 for this exact pairing — ABL1 and chronic myelogenous leukemia, BCR-ABL1 positive. The score reflects how much evidence of that kind exists and how consistent it is. It is not a probability that the drug works. Rows are ordered by how much each kind counts toward the evidence figure used in the ranking, not by its raw score, because the two disagree: literature co-occurrence saturates near 1.00 on almost any well-studied pair, while genetic association rarely exceeds 0.70 even when causal.

Genetic association0.86 / 1.00

Inherited variants in this gene alter disease risk in human populations. The datatype most predictive of later clinical success.55% of evidence score

Somatic mutation0.60 / 1.00

This gene is recurrently mutated in this tumour type.15% of evidence score

Animal model0.53 / 1.00

Altering this gene in animals reproduces or relieves the disease phenotype.15% of evidence score

Pathway0.97 / 1.00

The gene sits in a pathway with established disruption in this condition.8% of evidence score

Curated genetic literature0.61 / 1.00

Gene–disease links curated from published genetic studies.5% of evidence score

Literature co-occurrence1.00 / 1.00

Gene and condition appear together in published text. Reflects publication volume, not causal evidence.2% of evidence score

Clinical0.99 / 1.00

Derived from clinical or trial records.not counted

Phase 2 done, then stopped

A Phase 2 trial finished and was not followed by Phase 3. Dosing and safety in this population are already established.

NCT00254423 Dasatinib in Treating Patients With Earl · Ph 2 · 150 people

+14 more on ClinicalTrials.gov

What would kill it. A null trial, or pharmacokinetic data showing the drug does not reach ABL1 in the relevant tissue at tolerated doses.

piebaldism

Rejected — wrong way

It would be expected to worsen this condition. The genetic evidence indicates this condition requires the opposite modulation of the target. Shown rather than filtered so the direction check can be audited.

The condition

Piebaldism is a rare congenital pigmentation skin disorder characterized by the presence of hypopigmented and depigmented skin areas (leukoderma) on various parts of the body, preferentially on the forehead, chest, abdomen, upper arms, and lower extremities, that are associated with a white forelock (poliosis), and in some cases with hypopigmented and depigmented eyebrows and eyelashes.

KIT · KIT proto-oncogene, receptor tyrosine kinase

Open Targets scores each kind of evidence from 0.00 to 1.00 for this exact pairing — KIT and piebaldism. The score reflects how much evidence of that kind exists and how consistent it is. It is not a probability that the drug works. Rows are ordered by how much each kind counts toward the evidence figure used in the ranking, not by its raw score, because the two disagree: literature co-occurrence saturates near 1.00 on almost any well-studied pair, while genetic association rarely exceeds 0.70 even when causal.

Genetic association0.91 / 1.00

Inherited variants in this gene alter disease risk in human populations. The datatype most predictive of later clinical success.55% of evidence score

Animal model0.56 / 1.00

Altering this gene in animals reproduces or relieves the disease phenotype.15% of evidence score

Curated genetic literature0.72 / 1.00

Gene–disease links curated from published genetic studies.5% of evidence score

Literature co-occurrence0.05 / 1.00

Gene and condition appear together in published text. Reflects publication volume, not causal evidence.2% of evidence score

Nobody has tried this

No registered trial of this drug in this condition.

What would kill it. Direction conflict, unless the variant has been assigned the wrong functional class — a known failure mode of consequence-based annotation.

cutaneous mastocytosis

Rejected — wrong way

The condition

Cutaneous mastocytosis is a term referring to a group of diseases characterized by abnormal accumulation and proliferation of skin mastocytes. In some cases (most commonly in adults), cutaneous mastocytosis may occur in association with mast cell infiltration of various extracutaneous organs, in which case the disorder is referred to as systemic mastocytosis.

KIT · KIT proto-oncogene, receptor tyrosine kinase

Open Targets scores each kind of evidence from 0.00 to 1.00 for this exact pairing — KIT and cutaneous mastocytosis. The score reflects how much evidence of that kind exists and how consistent it is. It is not a probability that the drug works. Rows are ordered by how much each kind counts toward the evidence figure used in the ranking, not by its raw score, because the two disagree: literature co-occurrence saturates near 1.00 on almost any well-studied pair, while genetic association rarely exceeds 0.70 even when causal.

Genetic association0.92 / 1.00

Inherited variants in this gene alter disease risk in human populations. The datatype most predictive of later clinical success.55% of evidence score

Somatic mutation0.67 / 1.00

This gene is recurrently mutated in this tumour type.15% of evidence score

Animal model0.64 / 1.00

Altering this gene in animals reproduces or relieves the disease phenotype.15% of evidence score

Curated genetic literature0.76 / 1.00

Gene–disease links curated from published genetic studies.5% of evidence score

Literature co-occurrence0.52 / 1.00

Gene and condition appear together in published text. Reflects publication volume, not causal evidence.2% of evidence score

Clinical0.43 / 1.00

Derived from clinical or trial records.not counted

Nobody has tried this

No registered trial of this drug in this condition.

What would kill it. Direction conflict, unless the variant has been assigned the wrong functional class — a known failure mode of consequence-based annotation.

bilateral striopallidodentate calcinosis

Rejected — wrong way

The condition

A basal ganglia disease characterized by the accumulation of calcium deposits in different brain regions, particularly the basal ganglia and dentate nucleus, and is often associated with neurodegeneration.

PDGFRB · platelet derived growth factor receptor beta

Tyrosine-protein kinase that acts as a cell-surface receptor for homodimeric PDGFB and PDGFD and for heterodimers formed by PDGFA and PDGFB, and plays an essential role in the regulation of embryonic development, cell proliferation, survival, differentiation, chemotaxis and migration. Plays an essential role in blood vessel development by promoting proliferation, migration and recruitment of pericytes and smooth muscle cells to endothelial cells. Plays a role in the migration of vascular smooth muscle cells and the

Open Targets scores each kind of evidence from 0.00 to 1.00 for this exact pairing — PDGFRB and bilateral striopallidodentate calcinosis. The score reflects how much evidence of that kind exists and how consistent it is. It is not a probability that the drug works. Rows are ordered by how much each kind counts toward the evidence figure used in the ranking, not by its raw score, because the two disagree: literature co-occurrence saturates near 1.00 on almost any well-studied pair, while genetic association rarely exceeds 0.70 even when causal.

Genetic association0.85 / 1.00

Inherited variants in this gene alter disease risk in human populations. The datatype most predictive of later clinical success.55% of evidence score

Animal model0.51 / 1.00

Altering this gene in animals reproduces or relieves the disease phenotype.15% of evidence score

Somatic mutation0.21 / 1.00

This gene is recurrently mutated in this tumour type.15% of evidence score

Curated genetic literature0.83 / 1.00

Gene–disease links curated from published genetic studies.5% of evidence score

Literature co-occurrence0.47 / 1.00

Gene and condition appear together in published text. Reflects publication volume, not causal evidence.2% of evidence score

Nobody has tried this

No registered trial of this drug in this condition.

What would kill it. Direction conflict, unless the variant has been assigned the wrong functional class — a known failure mode of consequence-based annotation.

Why nobody will fund it

8 companies make this across 48 approved products. With that many manufacturers the price has fallen to production cost. A company funding a trial could not recover it — competitors could market the same molecule for the new indication immediately, without contributing.

How abandoned it is18 / 100

0 to 100, calculated from manufacturer count, remaining patent or exclusivity, and whether any reformulation route to exclusivity is still open. 100 means no route to commercial return exists. The weights behind it are unsourced.

THE ONE WAY A COMPANY COULD STILL OWN IT

injectableinhaledmodified-release

A new route or dosage form qualifies for a 505(b)(2) application, which carries three years of exclusivity for that formulation. It is the only remaining route to exclusivity on a generic molecule.

What it would cost to find out

Derived, not quoted. Events needed is 4(z_α+z_β)²/ln(HR)²; enrolment is that divided by the event rate and follow-up. The 1/ln(HR)² term dominates: halving the detectable effect size roughly quadruples enrolment. derived

Effect sought (hazard ratio)0.75

Lower = bigger effect = smaller trial

How often the event happens per year8.0%

Follow-up2 yr

Cost per patient$32K

Unsourced placeholder

379

Events needed

Patients

$93M

Trial cost

assumed

$5.93

Per person reached

assumed

Cost per person reached is the relevant metric for a non-commercial funder, since there is no revenue to set against the outlay.

Ask for ideas nobody has listed

Reasons from the functional groups and distribution above, excluding conditions already listed. Output is hypotheses for falsification, not findings. Not medical advice.

Who might pay for the trial

Trials of off-patent drugs are rarely funded by venture capital or pharma. They are paid for by government grants and disease foundations. Here is who has funded work on this molecule before, what federal mechanisms are open now, and which foundations fund trials in the disease areas it touches. measured

Federal grants that name this medicine

500 grants on NIH RePORTER

5R01AG073341-05(NIA · National Institute on Aging)Active

$645K (2026)

Reverse Engineering of Cell Senescence

PI: Kirschner, Marc Wallace · Harvard Medical School, Boston, MA · through 2026-11

View on NIH RePORTER ↗Apply to same mechanism (PA-20-185) ↗

5R01CA281984-03(NCI · National Cancer Institute)Active

$658K (2026)

Brain-Restricted Kinase Inhibition with Binary Pharmacology

PI: Weiss, William A · University Of California, San Francisco, San Francisco, CA · through 2029-02

View on NIH RePORTER ↗Apply to same mechanism (PA-20-185) ↗

5R33CA291301-03(NCI · National Cancer Institute)Active

$396K (2026)

Develop and validate demineralized bone paper-based human bone metabolic and senolytic assays

PI: Lee, Jungwoo · University Of Massachusetts Amherst, Hadley, MA · through 2027-07

View on NIH RePORTER ↗Apply to same mechanism (RFA-CA-23-003) ↗

See all 500 projects on NIH RePORTER →

Open federal programmes that would fund this work

Open notices with an explicit mandate to fund work on approved or off-patent molecules.

RFA-CA-25-033National Institutes of HealthForecast — not open yet

Glioblastoma Therapeutics Network (GTN; U19 Clinical Trial Required)

Grants.gov (RFA-CA-25-033) ↗Direct listing ↗Who already holds this grant ↗

RFA-FD-25-020Food and Drug Administrationcloses 05/16/2028

Reissue of RFA-FD-23-001- Clinical Studies of Orphan Products Addressing Unmet

Read announcement ↗Grants.gov (RFA-FD-25-020) ↗Direct listing ↗Who already holds this grant ↗

FOR-FD-25-020Food and Drug AdministrationForecast — not open yet

Clinical Studies of Orphan Products Addressing Unmet Needs of Rare Diseases (R

Grants.gov (FOR-FD-25-020) ↗Direct listing ↗Who already holds this grant ↗

FOR-FD-25-001Food and Drug AdministrationForecast — not open yet

Clinical Trials Addressing Unmet Needs of Rare Neurodegenerative Diseases (R01

Grants.gov (FOR-FD-25-001) ↗Direct listing ↗Who already holds this grant ↗

RFA-TR-25-002National Institutes of Healthcloses 07/02/2027

Preclinical Proof of Concept Studies for Rare Diseases (R21 Clinical Trial Not

Read announcement ↗Grants.gov (RFA-TR-25-002) ↗Direct listing ↗Who already holds this grant ↗

PAR-25-374National Institutes of Healthcloses 05/07/2028

Translational Bioinformatics and Experimental Approaches to Advance Drug Repos

Read announcement ↗Grants.gov (PAR-25-374) ↗Direct listing ↗Who already holds this grant ↗

HT942526PRCRPCTADefense Health Agency Contracting Activity -closes 10/05/2026

DoW Peer Reviewed Cancer, Clinical Trial Award

Grants.gov (HT942526PRCRPCTA) ↗Direct listing ↗Who already holds this grant ↗

PAR-26-049National Institutes of HealthForecast — not open yet

Establishing Pediatric CNS Pharmacodynamic Measures as Tools to Enable Psychia

Grants.gov (PAR-26-049) ↗Direct listing ↗Who already holds this grant ↗

Showing 8 of 990 currently open under this category on Grants.gov, matched to the disease areas this drug touches. derived Browse all 990 on Grants.gov ↗

Funders beyond the federal system

Grants.gov lists US federal money. Many off-patent drug trials are supported by disease foundations and nonprofits. These are matched to the body systems this drug touches. assumed

Matched by disease area, not by molecule — a foundation appearing here funds work in a field this drug touches.

Who manufactures it

Companies holding an approved abbreviated application for this molecule in the United States, from the FDA Orange Book. Supply already exists at scale, so a trial would not need a manufacturing programme — but any of these could also be a partner, or an objector.

Alembic Pharmaceuticals LtdApotex IncBiocon Pharma Ltd

Manufacturers

companies with their own approval

Approved products

distinct strengths and forms

Routes

oral

2006

Oldest product still sold

approval year of the earliest product still on the market

ALSO SOLD AS

PHYRAGOSPRYCEL

Nothing on this page is medical advice. Candidate uses are unproven hypotheses derived from public data; established uses are listed for verification only. Figures carry their provenance inline — anything marked assumed or derived is not a measurement.

← Back to the full ledger

What it's made of

Basic amine

Aromatic halogen

Where it can get to

What it binds — and whether we can reach it · 8 of 7 reachable

New uses, and who is already trying them

gastrointestinal stromal tumor

chronic myelogenous leukemia, BCR-ABL1 positive

piebaldism

cutaneous mastocytosis

bilateral striopallidodentate calcinosis

Why nobody will fund it

What it would cost to find out

Ask for ideas nobody has listed

Who might pay for the trial

Who manufactures it

Closely related medicines