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Cumberland Pharmaceuticals (CPIX) Q1 2026 Earnings Report

CPIX Q1 2026 EPS Results

Actual EPS
-$0.22
Consensus EPS
―
Beat/Miss
―
One Year Ago EPS
$0.08

CPIX Q1 2026 Revenue Results

Actual Revenue
$9.13M
Expected Revenue
―
Beat/Miss
―
YoY Revenue Growth
-22.04%

Earnings Announcement Details

Quarter
Q1 2026
Date
05/05/2026
Time
After Close
Conference Call
Tuesday, May 5, 2026
CPIX Upcoming Earnings

Cumberland Pharmaceuticals's next earnings date is estimated for November 10, 2026, based on past reporting schedules.

Q1 2026 Earnings Call Audio

CPIX Q1 2026 Earnings Call
0:00 / 0:00

Q1 2026 Earnings Slide Deck

No slide deck is available for this earnings event.

Q1 2026 Earnings Call Summary

Q1 2026
Earnings Call Date:May 05, 2026|% Change Since:32.94%|
Earnings Call Sentiment|Positive

The call highlights meaningful strategic progress: a transformational $100M acquisition agreement that unlocks near-term value, regulatory wins (expanded Caldolor label and facility clearance), commercialization progress (Talicia promotion, Vibativ China shipment) and an encouraging development pipeline (ifetroban with Fast Track and robust safety data). These positives are tempered by a modest Q1 revenue base, a GAAP net loss (~$3.3M) and limited cash on hand until the transaction closes, plus the company’s deliberate pivot away from pursuing double-digit revenue growth in 2026. On balance, the call emphasizes value realization and a clear strategic plan to focus on development, with the transaction expected to materially strengthen the balance sheet and reduce operating expense burden—leading to a favorable overall tone.

Company Guidance

Management guided that, given the announced strategic transaction with Apotex, Cumberland is no longer targeting double‑digit revenue growth for 2026 and expects materially lower operating expenses after closing because Apotex will assume sales, marketing, medical, manufacturing and FDA fees; at closing Cumberland expects $100 million cash (subject to shareholder approval), $9 million for inventory, ongoing monthly transition service fees and future milestone payments. For context, Q1 combined brand revenue was $9.1 million (Kristalose $1.0M; Sancuso $2.9M; Vibativ $2.1M; Caldolor $1.0M; Talicia $1.9M), total operating expenses were $12.3M, net loss was about $3.3M, adjusted loss was $1.9M or $0.13 per share, cash flow from operations was $0.387M, total assets were $71M (cash $11M), liabilities $49.7M (including $5M credit facility) and shareholders’ equity $21.6M. Management also said 2026 clinical spending is expected to remain essentially unchanged, noted over $53M of tax net operating losses versus a $30M tax basis in the assets (supporting modest taxes on the deal), and highlighted pipeline progress (ifetroban dosed in ~1,400 subjects, Fast Track/orphan/rare pediatric designations) and product milestones such as FDA‑expanded Caldolor labeling and a Vaprisol relaunch expected this year.

  • Transformational Strategic Transaction with ApotexApotex will acquire Cumberland's marketed U.S. commercial portfolio for $100 million in cash at closing, plus $9 million for inventory, transition service fees and a future sales-tied milestone — a transaction management expects will materially strengthen the balance sheet and unlock near-term shareholder value.
  • Revenue Performance and Product MixCombined Q1 2026 revenue from FDA-approved brands was $9.1 million (a 5% increase versus the comparable basis after excluding a $3 million one-time milestone in the prior year). Product-level Q1 revenue: Sancuso $2.9M, Vibativ $2.1M, Talicia $1.9M, Kristalose $1.0M and Caldolor $1.0M.
  • Pipeline Momentum — Ifetroban Clinical ProgressIfetroban has been dosed in ~1,400 subjects with an outstanding safety database; positive Phase II top-line DMD results announced previously; FDA granted Fast Track designation for Duchenne muscular dystrophy and the program also holds orphan and rare pediatric disease designations. Ongoing trials include completed enrollment in systemic sclerosis and active enrollment in the idiopathic pulmonary fibrosis 'Fighting Fibrosis' Phase II trial (interim safety review found no new safety signals).
  • Regulatory and Commercial Advances for Branded ProductsFDA approved expanded labeling for Caldolor to include postoperative pain (use in adults and pediatric patients 3 months+), FDA cleared the manufacturing facility enabling Vaprisol relaunch this year, and the first shipment of Vibativ to China occurred. Cumberland also launched national sales promotion for Talicia and updated Sancuso's website.
  • Positive Operating Cash Flow Despite Seasonal QuarterCumberland generated positive cash flow from operations of $387,000 in Q1 2026, reflecting improving cash generation from the recently acquired brands and ongoing commercialization efforts.
  • Balance Sheet and Tax PositionAs of 3/31/2026 Cumberland reported $71M in total assets (including $11M cash), $49.7M in liabilities and $21.6M in shareholders' equity. Management cites >$53M in tax net operating loss carryforwards and a $30M tax basis in transaction assets, which is expected to limit transaction-related income taxes.

CPIX Earnings History

CPIX earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Nov 10, 20262026 (Q3)―--0.13――
Aug 04, 20262026 (Q2)―-0.28-0.05-470.00% (-0.23)
May 05, 20262026 (Q1)―-0.220.08-368.29% (-0.30)
Mar 03, 20262025 (Q4)―-0.09-0.1430.88% (+0.04)
Nov 04, 20252025 (Q3)―-0.13-0.11-18.18% (-0.02)
Aug 05, 20252025 (Q2)―-0.05-0.0835.06% (+0.03)
May 06, 20252025 (Q1)―0.08-0.14159.42% (+0.22)
Mar 04, 20252024 (Q4)―-0.14-0.4469.37% (+0.31)
Nov 07, 20242024 (Q3)―-0.11-0.07-48.65% (-0.04)
Aug 06, 20242024 (Q2)―-0.080.06-228.33% (-0.14)

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
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