Market Cap 566.84M
Revenue (ttm) 0.00
Net Income (ttm) -324.25M
EPS (ttm) N/A
PE Ratio 0.00
Forward PE N/A
Profit Margin 0.00%
Debt to Equity Ratio 0.00
Volume 747,800
Avg Vol 396,386
Day's Range N/A - N/A
Shares Out 54.14M
Stochastic %K 98%
Beta N/A
Analysts Strong Sell
Price Target $24.60

Company Profile

Eikon Therapeutics, Inc., operates as a clinical biopharmaceutical company in the United States. It develops medicines to address serious unmet medical needs. Its products include EIK1001, a systemically administered TLR 7/8 dual-agonist designed to activate innate and adaptive immune anti-tumor responses; EIK1003 and EIK1004, which are selective PARP1 inhibitors in ovarian, breast, prostate, and pancreatic cancers and, specifically with the brain-penetrant; EIK1004 to address brain metastases a...

Industry: Biotechnology
Sector: Healthcare
Phone: 341 777 0566
Website: eikontx.com
Address:
230 Harriet Tubman Way, Millbrae, United States
stockydennis
stockydennis Aug. 19 at 11:29 AM
$EIKN booking my punta cana trip now
0 · Reply
Gurujoe
Gurujoe Aug. 17 at 5:42 PM
$EIKN— Why ESMO Could Be a Major Pipeline Re-Rating Event Eikon’s 7 ESMO abstracts matter less for quantity than for quality: several datasets now reflect more biologically selected, expanded cohorts, which may improve efficacy versus earlier readouts. ──────── EIK1001 — 1L NSCLC (Oct 26 | Primary Value Driver) ASCO Baseline Data • Pooled ORR: 63.1% • DCR: 90.8% • Squamous cohort: 72.4% ORR / 100% DCR • Median follow-up: 8.8 months (squamous) • Non-squamous DOR: >11 months (early signal) ESMO Focus • Durability of 72.4% squamous ORR • Conversion of response into PFS / DOR maturity • Squamous vs non-squamous separation • Evidence of response deepening or plateauing Why It Matters • Lead asset and largest rNPV contributor • Oct 26 is the key catalyst • Durability confirmation could materially shift PoS assumptions ──────── EIK1003 — Selective PARP1 Inhibitor Monotherapy / Breast Cancer ASCO Baseline Data • ORR: 14.3% • PARPi-naïve subgroup: 26.7% ORR ESMO Focus • Validation of 25–30%+ ORR in enriched PARPi-naïve cohorts • Dose response (20 mg vs 60 mg) • Consistency in HER2-negative breast cancer Why It Matters • Highlights importance of biological enrichment • Mixed-population ORR likely understates true activity • Could reposition drug as subgroup-selective high-activity therapy ──────── EIK1003 + Paclitaxel (Ovarian / Combination) ASCO Baseline Data • ORR: 24.5% • Platinum-resistant ovarian cancer: 29.6% ORR • Prior taxane exposure: 92% of responders ESMO Focus • Cohort 1D (platinum + paclitaxel) • Maintenance of ~25–30% ORR range • Combination safety profile Why It Matters • Tests PARP1 selectivity under chemo pressure • If maintained, supports chemo-stackability • Expands ovarian franchise potential ──────── EIK1003 — Prostate (Oct 23 Readout) ESMO Focus • PSA50 response rate • Early RECIST activity • PSA durability Why It Matters • First expansion beyond breast/ovarian • Validates multi-franchise potential • Expands peak TAM optionality ──────── EIK1004 — CNS-Penetrant PARP1 (Oct 23) ESMO Focus • CNS penetration / PK profile • Safety and tolerability • Intracranial or CNS tumor activity Why It Matters • Rare CNS-active PARP-class asset • Positive signal opens neuro-oncology expansion • High optionality despite early stage ──────── EIK1005 — WRN Inhibitor (Oct 23) ESMO Focus • Dose escalation and safety • PK/PD validation in MSI-H/dMMR tumors • Early biomarker signals Why It Matters • Expands into synthetic lethality beyond PARP • Platform validation stage • Not yet efficacy-driven ──────── ESMO Catalyst Timeline Oct 23 — Platform Expansion (Medium Impact Overall) • EIK1003 (Prostate Combo) → Medium impact • PSA50, early response signals • First non-breast/ovarian validation • EIK1004 (CNS PARP1) → Medium–High (if CNS signal emerges) • Brain penetration, intracranial activity • Potential CNS oncology entry • EIK1005 (WRN) → Low–Medium impact • Safety, PK, early PD markers • Platform expansion signal ──────── Oct 26 — Core Value Driver (High Impact) • EIK1001 (1L NSCLC expansion) → VERY HIGH impact • Squamous durability (72.4% ORR sustainability) • DOR/PFS maturation • Cohort consistency Why It Matters • Primary rNPV driver • Most important near-term catalyst • Durability confirmation could re-rate probability assumptions ──────── Valuation Framework (Scenario-Based) • Base pipeline rNPV: ~$2.5B • Constructive ESMO: ~$2.4–2.8B implied value • Bull case (multi-asset validation): ~$4–5B implied value Not price targets—scenario outputs. ──────── Balance Sheet Context • Cash & marketable securities: $531.2M • Q2 R&D: $75.5M • Net loss: $88.4M • Runway: into 2H 2027 ──────── Key Takeaway ESMO does not require universal success across programs. The key sensitivities are: • EIK1001 durability (NSCLC squamous cohort) • EIK1003 validation in PARPi-naïve enriched populations If both hold, the market may begin assigning independent high-confidence probabilities across multiple assets, a typical trigger for pipeline re-rating. Core insight: the datasets are not just larger — they are more biologically selected, creating asymmetric upside potential. NFA/DYOD (Not Financial Advice/Do Your Own Due Diligence ).
0 · Reply
LW199
LW199 Aug. 17 at 1:00 AM
$MRK Why nobody is talking about $EIKN ? It is seen as merck 2.0… eik1001 could be a big game changer.
0 · Reply
Gurujoe
Gurujoe Aug. 13 at 10:13 PM
$EIKN - Q2: Funded Into Major 7-Abstract ESMO Catalyst Eikon finished Q2 with $531.2M cash and runway into 2H27. No debt or preferred stock, although ~$252M of $313M liabilities are operating leases, so it’s not a pure net-cash story. The bigger story is ESMO 2026, where Eikon has seven accepted abstracts spanning four clinical assets: 2 EIK1001, 2 EIK1003, 1 EIK1004 and 2 EIK1005. That breadth matters. This isn’t simply another update on the lead EIK1001 program. ESMO provides multiple opportunities to establish value across the pipeline: * EIK1003: updated monotherapy/paclitaxel data plus the first abiraterone combination data in metastatic prostate cancer. * EIK1004: first-in-human data for the CNS-penetrant PARP1 inhibitor. * EIK1005: initial clinical safety/tolerability/PK data for Eikon’s internally developed WRN inhibitor, plus its Phase 1/2 monotherapy/KEYTRUDA program. * EIK1001: updated TeLuRide-005 NSCLC results plus TeLuRide-008 registrational-program presentation. The implication: seven abstracts across four drugs gives Eikon multiple shots on goal. Strong data from EIK1003/1004/1005 could begin shifting the valuation from primarily EIK1001 toward a multi-asset oncology platform, while weak early data could challenge that pipeline-premium thesis. That makes Oct. 23 particularly important: multiple datasets, including first clinical looks at previously unproven assets, can start answering whether Eikon has genuine pipeline breadth rather than one lead program plus optionality. Q2 shows they have the cash to get there. ESMO starts showing what the pipeline may actually be worth. NFAD/DYOR.
0 · Reply
stockydennis
stockydennis Aug. 11 at 7:38 PM
$EIKN I think I smell news idk I feel it
0 · Reply
STACKD0E
STACKD0E Aug. 11 at 12:25 PM
$EIKN 🙃✨️
0 · Reply
STACKD0E
STACKD0E Aug. 11 at 12:06 PM
0 · Reply
justiceforb_85
justiceforb_85 Jul. 29 at 1:27 AM
$EIKN trading below cash seems a bit extreme. Update for EIKN-1001 in melanoma (randomized data) planned for later this year?
0 · Reply
ajmrtxl
ajmrtxl Jul. 27 at 3:37 PM
$EIKN 's latest data on SqueezeFinder
0 · Reply
stockydennis
stockydennis Jul. 27 at 3:02 PM
$EIKN perfect
0 · Reply
Latest News on EIKN
Eikon Therapeutics reports Q2 EPS ($1.63), consensus ($1.46)

2026-08-16T14:07:43.000Z - 2 days ago

Eikon Therapeutics reports Q2 EPS ($1.63), consensus ($1.46)


Eikon Therapeutics Slides: Investor presentation

Aug 14, 2026, 7:00 AM EDT - 5 days ago

Eikon Therapeutics Slides: Investor presentation


Eikon Therapeutics Quarterly report: Q2 2026

Aug 13, 2026, 4:00 PM EDT - 5 days ago

Eikon Therapeutics Quarterly report: Q2 2026


Eikon Therapeutics Earnings release: Q2 2026

Aug 13, 2026, 4:00 PM EDT - 5 days ago

Eikon Therapeutics Earnings release: Q2 2026


Eikon Therapeutics Slides: Company presentation

Jul 27, 2026, 9:00 AM EDT - 22 days ago

Eikon Therapeutics Slides: Company presentation


Eikon Therapeutics doses first patient in TeLuRide-008 study

2026-07-27T12:02:02.000Z - 22 days ago

Eikon Therapeutics doses first patient in TeLuRide-008 study


Eikon Therapeutics to be added to Russell 3000 Index

2026-06-25T20:25:09.000Z - 7 weeks ago

Eikon Therapeutics to be added to Russell 3000 Index


Eikon Therapeutics to Join the Russell 3000® Index

Jun 25, 2026, 4:15 PM EDT - 7 weeks ago

Eikon Therapeutics to Join the Russell 3000® Index


Eikon Therapeutics price target lowered to $32 from $34 at BofA

2026-06-03T15:20:40.000Z - 2 months ago

Eikon Therapeutics price target lowered to $32 from $34 at BofA


Eikon Therapeutics presents data on lead programs at ASCO 2026

2026-05-31T21:10:05.000Z - 2 months ago

Eikon Therapeutics presents data on lead programs at ASCO 2026


Eikon Therapeutics Earnings release: Q1 2026

May 11, 2026, 4:00 PM EDT - 3 months ago

Eikon Therapeutics Earnings release: Q1 2026


Eikon Therapeutics Quarterly report: Q1 2026

May 11, 2026, 4:00 PM EDT - 3 months ago

Eikon Therapeutics Quarterly report: Q1 2026


Eikon Therapeutics Earnings release: Q4 2025

Mar 30, 2026, 8:00 AM EDT - 5 months ago

Eikon Therapeutics Earnings release: Q4 2025


Eikon Therapeutics Annual report: Q4 2025

Mar 30, 2026, 8:00 AM EDT - 5 months ago

Eikon Therapeutics Annual report: Q4 2025


Eikon Therapeutics initiated with a Buy at BofA

2026-03-02T11:53:21.000Z - 6 months ago

Eikon Therapeutics initiated with a Buy at BofA


Eikon Therapeutics initiated with an Outperform at Mizuho

2026-03-02T10:25:23.000Z - 6 months ago

Eikon Therapeutics initiated with an Outperform at Mizuho


Eikon Therapeutics initiated with an Overweight at JPMorgan

2026-03-02T10:15:23.000Z - 6 months ago

Eikon Therapeutics initiated with an Overweight at JPMorgan


Eikon Therapeutics initiated with an Underperform at Wedbush

2026-02-26T11:49:40.000Z - 6 months ago

Eikon Therapeutics initiated with an Underperform at Wedbush


Eikon Therapeutics valued at $860 million in Nasdaq debut

Feb 5, 2026, 12:47 PM EST - 6 months ago

Eikon Therapeutics valued at $860 million in Nasdaq debut


Eikon Therapeutics opens at $17.05, IPO priced at $18.00

2026-02-05T17:45:13.000Z - 6 months ago

Eikon Therapeutics opens at $17.05, IPO priced at $18.00


Eikon Therapeutics Registration statement: Registration Filing

Jan 28, 2026, 7:00 AM EST - 7 months ago

Eikon Therapeutics Registration statement: Registration Filing


Eikon ‍Therapeutics targets $908 million valuation in US IPO

Jan 28, 2026, 6:19 AM EST - 7 months ago

Eikon ‍Therapeutics targets $908 million valuation in US IPO


Biopharmaceutical firm Eikon Therapeutics files for US IPO

Jan 9, 2026, 4:24 PM EST - 7 months ago

Biopharmaceutical firm Eikon Therapeutics files for US IPO


Eikon Therapeutics IPO Registration Document (S-1)

Jan 9, 2026, 4:02 PM EST - 7 months ago

Eikon Therapeutics IPO Registration Document (S-1)


stockydennis
stockydennis Aug. 19 at 11:29 AM
$EIKN booking my punta cana trip now
0 · Reply
Gurujoe
Gurujoe Aug. 17 at 5:42 PM
$EIKN— Why ESMO Could Be a Major Pipeline Re-Rating Event Eikon’s 7 ESMO abstracts matter less for quantity than for quality: several datasets now reflect more biologically selected, expanded cohorts, which may improve efficacy versus earlier readouts. ──────── EIK1001 — 1L NSCLC (Oct 26 | Primary Value Driver) ASCO Baseline Data • Pooled ORR: 63.1% • DCR: 90.8% • Squamous cohort: 72.4% ORR / 100% DCR • Median follow-up: 8.8 months (squamous) • Non-squamous DOR: >11 months (early signal) ESMO Focus • Durability of 72.4% squamous ORR • Conversion of response into PFS / DOR maturity • Squamous vs non-squamous separation • Evidence of response deepening or plateauing Why It Matters • Lead asset and largest rNPV contributor • Oct 26 is the key catalyst • Durability confirmation could materially shift PoS assumptions ──────── EIK1003 — Selective PARP1 Inhibitor Monotherapy / Breast Cancer ASCO Baseline Data • ORR: 14.3% • PARPi-naïve subgroup: 26.7% ORR ESMO Focus • Validation of 25–30%+ ORR in enriched PARPi-naïve cohorts • Dose response (20 mg vs 60 mg) • Consistency in HER2-negative breast cancer Why It Matters • Highlights importance of biological enrichment • Mixed-population ORR likely understates true activity • Could reposition drug as subgroup-selective high-activity therapy ──────── EIK1003 + Paclitaxel (Ovarian / Combination) ASCO Baseline Data • ORR: 24.5% • Platinum-resistant ovarian cancer: 29.6% ORR • Prior taxane exposure: 92% of responders ESMO Focus • Cohort 1D (platinum + paclitaxel) • Maintenance of ~25–30% ORR range • Combination safety profile Why It Matters • Tests PARP1 selectivity under chemo pressure • If maintained, supports chemo-stackability • Expands ovarian franchise potential ──────── EIK1003 — Prostate (Oct 23 Readout) ESMO Focus • PSA50 response rate • Early RECIST activity • PSA durability Why It Matters • First expansion beyond breast/ovarian • Validates multi-franchise potential • Expands peak TAM optionality ──────── EIK1004 — CNS-Penetrant PARP1 (Oct 23) ESMO Focus • CNS penetration / PK profile • Safety and tolerability • Intracranial or CNS tumor activity Why It Matters • Rare CNS-active PARP-class asset • Positive signal opens neuro-oncology expansion • High optionality despite early stage ──────── EIK1005 — WRN Inhibitor (Oct 23) ESMO Focus • Dose escalation and safety • PK/PD validation in MSI-H/dMMR tumors • Early biomarker signals Why It Matters • Expands into synthetic lethality beyond PARP • Platform validation stage • Not yet efficacy-driven ──────── ESMO Catalyst Timeline Oct 23 — Platform Expansion (Medium Impact Overall) • EIK1003 (Prostate Combo) → Medium impact • PSA50, early response signals • First non-breast/ovarian validation • EIK1004 (CNS PARP1) → Medium–High (if CNS signal emerges) • Brain penetration, intracranial activity • Potential CNS oncology entry • EIK1005 (WRN) → Low–Medium impact • Safety, PK, early PD markers • Platform expansion signal ──────── Oct 26 — Core Value Driver (High Impact) • EIK1001 (1L NSCLC expansion) → VERY HIGH impact • Squamous durability (72.4% ORR sustainability) • DOR/PFS maturation • Cohort consistency Why It Matters • Primary rNPV driver • Most important near-term catalyst • Durability confirmation could re-rate probability assumptions ──────── Valuation Framework (Scenario-Based) • Base pipeline rNPV: ~$2.5B • Constructive ESMO: ~$2.4–2.8B implied value • Bull case (multi-asset validation): ~$4–5B implied value Not price targets—scenario outputs. ──────── Balance Sheet Context • Cash & marketable securities: $531.2M • Q2 R&D: $75.5M • Net loss: $88.4M • Runway: into 2H 2027 ──────── Key Takeaway ESMO does not require universal success across programs. The key sensitivities are: • EIK1001 durability (NSCLC squamous cohort) • EIK1003 validation in PARPi-naïve enriched populations If both hold, the market may begin assigning independent high-confidence probabilities across multiple assets, a typical trigger for pipeline re-rating. Core insight: the datasets are not just larger — they are more biologically selected, creating asymmetric upside potential. NFA/DYOD (Not Financial Advice/Do Your Own Due Diligence ).
0 · Reply
LW199
LW199 Aug. 17 at 1:00 AM
$MRK Why nobody is talking about $EIKN ? It is seen as merck 2.0… eik1001 could be a big game changer.
0 · Reply
Gurujoe
Gurujoe Aug. 13 at 10:13 PM
$EIKN - Q2: Funded Into Major 7-Abstract ESMO Catalyst Eikon finished Q2 with $531.2M cash and runway into 2H27. No debt or preferred stock, although ~$252M of $313M liabilities are operating leases, so it’s not a pure net-cash story. The bigger story is ESMO 2026, where Eikon has seven accepted abstracts spanning four clinical assets: 2 EIK1001, 2 EIK1003, 1 EIK1004 and 2 EIK1005. That breadth matters. This isn’t simply another update on the lead EIK1001 program. ESMO provides multiple opportunities to establish value across the pipeline: * EIK1003: updated monotherapy/paclitaxel data plus the first abiraterone combination data in metastatic prostate cancer. * EIK1004: first-in-human data for the CNS-penetrant PARP1 inhibitor. * EIK1005: initial clinical safety/tolerability/PK data for Eikon’s internally developed WRN inhibitor, plus its Phase 1/2 monotherapy/KEYTRUDA program. * EIK1001: updated TeLuRide-005 NSCLC results plus TeLuRide-008 registrational-program presentation. The implication: seven abstracts across four drugs gives Eikon multiple shots on goal. Strong data from EIK1003/1004/1005 could begin shifting the valuation from primarily EIK1001 toward a multi-asset oncology platform, while weak early data could challenge that pipeline-premium thesis. That makes Oct. 23 particularly important: multiple datasets, including first clinical looks at previously unproven assets, can start answering whether Eikon has genuine pipeline breadth rather than one lead program plus optionality. Q2 shows they have the cash to get there. ESMO starts showing what the pipeline may actually be worth. NFAD/DYOR.
0 · Reply
stockydennis
stockydennis Aug. 11 at 7:38 PM
$EIKN I think I smell news idk I feel it
0 · Reply
STACKD0E
STACKD0E Aug. 11 at 12:25 PM
$EIKN 🙃✨️
0 · Reply
STACKD0E
STACKD0E Aug. 11 at 12:06 PM
0 · Reply
justiceforb_85
justiceforb_85 Jul. 29 at 1:27 AM
$EIKN trading below cash seems a bit extreme. Update for EIKN-1001 in melanoma (randomized data) planned for later this year?
0 · Reply
ajmrtxl
ajmrtxl Jul. 27 at 3:37 PM
$EIKN 's latest data on SqueezeFinder
0 · Reply
stockydennis
stockydennis Jul. 27 at 3:02 PM
$EIKN perfect
0 · Reply
STACKD0E
STACKD0E Jul. 27 at 11:49 AM
$EIKN ✨️
0 · Reply
TA_Kongen
TA_Kongen Jul. 27 at 11:33 AM
$EIKN Another interesting biotech. Need more headlines/info though.
0 · Reply
stockydennis
stockydennis Jul. 24 at 5:34 PM
$EIKN volume is stupid low Merck arriving shortly
1 · Reply
topstockalerts
topstockalerts Jul. 13 at 1:15 PM
Pre Market Top Gainers PT2 $MIMI $EHGO $SOBR $SKYQ $EIKN
0 · Reply
arbwatson
arbwatson Jul. 9 at 5:45 PM
$EIKN slow and steady. Moving up.
1 · Reply
arbwatson
arbwatson Jul. 9 at 3:19 PM
$EIKN This company has some interesting trials. Someone needs to pop this thing.
0 · Reply
StockScanners
StockScanners Jun. 27 at 5:58 PM
$EIKN keep watch if this holds above 10.99
0 · Reply
topstockalerts
topstockalerts Jun. 12 at 12:12 PM
Pre Market Top Gainers PT2 $RUBI $EIKN $RKTO $EJH $JFU
0 · Reply
topstockalerts
topstockalerts Jun. 12 at 11:33 AM
Pre Market Top Gainers PT2 $RUBI $EIKN $RKTO $EJH $JFU
0 · Reply
SuperGreenToday
SuperGreenToday Jun. 11 at 9:14 PM
0 · Reply
Gurujoe
Gurujoe Jun. 2 at 11:26 PM
$EIKN — Quick context: market makers pressuring the entire small-cap biotech tape right now. XBI weak, low liquidity, algorithmic short-side activity, sector ETF outflows compounding. Quality names get mispriced in this environment because sector tape overwhelms individual fundamentals. Patience pays. Why EIKN remains a high-conviction long: SETUP: $10.52 / $570M mkt cap / $596M cash / ~zero EV / $11.02 cash floor / 22 mo runway. Stock literally trading below cash. Wedbush $5 PT vs Street consensus $25-34. ASCO 2026 DATA (May 30): • EIK1001 NSCLC: 63.1% pooled ORR (SQ 72.4% vs KN-407 ~58%); PD-L1 <1% (negative) subgroup 60% ORR (vs KN-189 historical ~32%); median DOR NSQ >11 mo • EIK1003 PARP1+PTX: 24.5% ORR; 92% of responders had prior taxane; first clinical proof PARP1-selectivity enables chemo combos THE MERCK SETUP — read the Fierce Pharma piece: May 30 Fierce Pharma article: “Sac-TMT’s massive Phase 3 program has a jarring gap. Does Merck plan to close it?” Merck has 17 Ph3 trials for sac-TMT but explicitly NO registrational study in 1L PD-L1 negative/low non-squamous NSCLC — the KEYNOTE-189 population. Fierce called the gap “jarring.” Marjorie Green (Merck head of oncology dev) to Fierce on the ASCO sidelines: “Everyone is like, ‘When are you going to replace 189?’” Her reasoning for the gap: sac-TMT is a topo-1 ADC and combining it with platinum chemo would require dose reductions that erode efficacy. Merck deliberately didn’t “throw the kitchen sink.” EIK1001 fits the PD-L1 negative gap exactly: • 60% ORR in PD-L1 <1% (vs KN-189 ~32%) — the exact segment Merck can’t reach with sac-TMT • TLR7/8 immune-activation is orthogonal to chemo, doesn’t compromise dosing — solves the exact problem Green identified • TeLuRide-008 reg trial PD-L1 stratified, Merck supplying pembro, designed to register the gap • Kenneth Frazier (former Merck CEO) on EIKN board • 3 ex-Merck execs in C-suite (Perlmutter, Baynes, Klobuchar) • Hoki (Merck Rahway) co-author on EIK1001 melanoma poster Probability-weighted Merck acquisition: 50-60% at $30-60/share within 24-36 mo. MONTE CARLO (10K iter): Median $13.65 (+30%) / Mean $15.55 (+48%) / P90 $32.18 (+206%) / + $15-30/share risk-adjusted M&A optionality. CATALYSTS: 8 milestones in 2H 2026 alone — EIK1001-006 interim, EIK1001-005 SQ mature, EIK1003 abiraterone, EIK1004 escalation complete, EIK1006 IND. Patience through tape weakness — catalyst path reveals value. NFAD. DYOR.
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