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Karyopharm Therapeutics (KPTI)
NASDAQ:KPTI
US Market
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Karyopharm Therapeutics (KPTI) Earnings Dates, Call Summary & Reports

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Earnings Data

Report Date
Jul 30, 2026
TBA (Confirmed)
Period Ending
2026 (Q2)
Consensus EPS Forecast
-1.31
Last Year’s EPS
-4.32
Same Quarter Last Year
Based on 7 Analysts Ratings

Earnings Call Summary

Q1 2026
Earnings Call Date:May 14, 2026|
% Change Since:
|
Earnings Call Sentiment|Positive
The call conveys strong clinical momentum and significant near-term catalysts: compelling Phase III SENTRY results with a statistically robust spleen response and an intriguing overall survival signal, completed enrollment in EC042 with prior SIENDO data showing deep and durable PFS benefit, ASCO presentation and planned mid-2026 manuscript, and quarter-over-quarter revenue improvement driven by gross-to-net gains. These positives are tempered by competitive pressure that reduced underlying demand for XPOVIO, gross-to-net volatility, continued net losses and high operating spend, and a limited cash runway into late Q3 2026 that may necessitate additional financing or milestone events. Regulatory timing and the need for further data granularity (e.g., deaths attribution) add some near-term uncertainty. On balance, the clinical and strategic highlights are material and potentially value-creating, though execution and financing risks remain.
Company Guidance
On the call Karyopharm reaffirmed full‑year 2026 financial guidance of total revenue $130–150M and U.S. XPOVIO net product revenue $115–130M, with combined R&D + SG&A expected to be $230–245M; Q1 results were $35.1M total revenue (vs. $30.0M a year ago), U.S. XPOVIO net product revenue $29.2M (vs. $21.1M), gross‑to‑net 21.8% (vs. 45% in Q1‑2025; ~26% underlying ex‑adjustments), R&D $33.8M, SG&A $26.7M, net loss $22.4M (vs. $23.5M) and a ~20% reduction in loss from operations, and cash/cash equivalents/restricted cash of $91.2M (including ~ $50M financing) providing runway into late Q3 2026; operational milestones and metrics include completed enrollment in EC042 with 257 ITT / ~220 MITT (primary analysis) and top‑line EC042 readout expected mid‑2026, Phase III SENTRY efficacy signals (SVR35 at week 24: 50% selinexor+ruxolitinib vs. 28% ruxolitinib, p<0.0001; OS HR 0.43, nominal p=0.0222; VAF reduction ≥20% in 32% of combo patients; spleen responses as early as week 12 sustained to week 36), prior SIENDO PFS in p53 wild‑type of 13.7 vs 3.7 months (HR 0.41) with long‑term selinexor PFS up to 28.4 months (HR 0.44) and p53 wt/MMR‑proficient PFS ~40 months (HR 0.36), and commercial sizing assumptions of ~20,000 MF patients alive, ~7,000 annual first‑line MF diagnoses (~4,000 addressable), ~17,000 annual advanced/recurrent endometrial cases, and a modeled U.S. MF peak revenue opportunity of ~ $1B.
SENTRY Phase III: Strong Spleen Volume Reduction (SVR35)
Co-primary SVR35 at week 24: 50% for selinexor + ruxolitinib vs 28% for ruxolitinib alone (p < 0.0001). Rapid meaningful spleen volume reductions observed as early as week 12 and sustained through week 36, indicating a durable effect.
Promising Overall Survival Signal and Disease-Modification Markers in SENTRY
Overall survival hazard ratio 0.43 (nominal p = 0.0222) favoring the combination. Post-hoc analyses show SVR35 predicts OS; 32% of combination patients had ≥20% variant allele frequency (VAF) reductions, consistent with potential disease modification.
Peer Recognition and Publication Plans
SENTRY data selected for a late-breaking oral presentation at ASCO; manuscript planned for a peer-reviewed journal in mid-2026, supporting scientific validation and visibility.
Endometrial Cancer Program: EC042 Enrollment Complete; SIENDO Benchmarks Very Positive
EC042 enrollment complete with 257 ITT and ~220 mITT (primary analysis population); top-line EC042 data expected mid-2026. Prior SIENDO data in p53 wild-type subgroup: median PFS 13.7 vs 3.7 months (HR 0.41) at top-line, extending to median PFS 28.4 months (HR 0.44) on long-term follow-up; p53 wild-type/MMR-proficient subgroup median PFS ~40 months (HR 0.36), comparing favorably to RUBY (HR 0.77).
Quarterly Revenue Growth and Gross-to-Net Improvement
Q1 total revenue $35.1M vs $30.0M year-ago (+~17%). U.S. XPOVIO net product revenue $29.2M vs $21.1M (+~38.4%). Gross-to-net decreased to 21.8% this quarter from 45.0% in Q1 2025 (improvement of ~23.2 percentage points); underlying gross-to-net estimated ~26% excluding atypical adjustments.
Improved Underlying Operating Performance and Confirmed Guidance
Net loss improved to $22.4M from $23.5M year-over-year. Company reports a 20% reduction in loss from operations on an underlying basis. Reaffirmed full-year 2026 guidance: total revenue $130M–$150M; U.S. XPOVIO net product revenue $115M–$130M; combined R&D + SG&A $230M–$245M.
Balance Sheet Strengthening and Commercial Readiness
Ended quarter with $91.2M cash, cash equivalents and restricted cash (including ~ $50M financing completed in March). Company emphasizes established commercial capabilities (sales, market access, medical affairs), community-focused coverage (≈60% of U.S. sales), and preparedness to launch in myelofibrosis and endometrial cancer with limited incremental pre-approval spend.
Commercial Market Opportunity
Addressable U.S. myelofibrosis market: ~20,000 living patients, ~7,000 newly diagnosed first-line annually (~4,000 addressable); company projects up to ~$1B U.S. peak annual revenue for selinexor + ruxolitinib. Endometrial advanced/recurrent pool ≈17,000 annually with ~50% p53 wild-type (substantial maintenance opportunity).

Karyopharm Therapeutics (KPTI) Earnings, Revenues Date & History

The upcoming earnings date is based on a company’s previous reporting, and may be updated when the actual date is announced

KPTI Earnings History

Report Date
Fiscal Quarter
Forecast / EPS
Last Year's EPS
EPS YoY Change
Press Release
Slides
Play Transcript
Jul 30, 2026
2026 (Q2)
-1.31 / -
-4.32
May 14, 2026
2026 (Q1)
-1.42 / -1.24
-2.7755.23% (+1.53)
Feb 12, 2026
2025 (Q4)
-1.99 / -5.71
-3.6-58.61% (-2.11)
Nov 03, 2025
2025 (Q3)
-3.47 / -3.82
-3.92.05% (+0.08)
Aug 11, 2025
2025 (Q2)
-4.08 / -4.32
-3-44.00% (-1.32)
May 12, 2025
2025 (Q1)
-4.42 / -2.77
-4.842.29% (+2.03)
Feb 19, 2025
2024 (Q4)
-3.92 / -3.60
-5.433.33% (+1.80)
Nov 05, 2024
2024 (Q3)
-3.94 / -3.90
-4.513.33% (+0.60)
Aug 06, 2024
2024 (Q2)
-4.47 / -3.00
-4.3531.03% (+1.35)
May 08, 2024
2024 (Q1)
-5.01 / -4.80
-4.5-6.67% (-0.30)
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.
Beat
Missed

KPTI Earnings-Related Price Changes

Report Date
Price 1 Day Before
Price 1 Day After
Percentage Change
May 14, 2026
$8.85$8.90+0.56%
Feb 12, 2026
$7.37$8.94+21.30%
Nov 03, 2025
$5.80$6.07+4.66%
Aug 11, 2025
$3.94$3.77-4.31%
Earnings announcements can affect a stock’s price. This table shows the stock's price the day before and the day after recent earnings reports, including the percentage change.

FAQ

When does Karyopharm Therapeutics (KPTI) report earnings?
Karyopharm Therapeutics (KPTI) is schdueled to report earning on Jul 30, 2026, TBA (Confirmed).
    What is Karyopharm Therapeutics (KPTI) earnings time?
    Karyopharm Therapeutics (KPTI) earnings time is at Jul 30, 2026, TBA (Confirmed).
      Where can I see when companies are reporting earnings?
      You can see which companies are reporting today on our designated earnings calendar.
        What companies are reporting earnings today?
        You can see a list of the companies which are reporting today on TipRanks earnings calendar.
          What is KPTI EPS forecast?
          KPTI EPS forecast for the fiscal quarter 2026 (Q2) is -1.31.