-
Cumberland delays release of FIGHT DMD ifetroban long-term data; no new timeline
Phase 2 FIGHT DMD open-label extension long-term safety/efficacy data for ifetroban not yet available.
-
Cumberland closes $100M Apotex deal, pays $1.50 special dividend, reports Q2 loss
Closed $100M strategic transaction with Apotex Health; received $111M total including inventory and transition services.
-
Cumberland Pharmaceuticals declares special dividend of $1.50/share, authorizes $5M buyback
Special cash dividend of $1.50 per share, payable July 31, 2026 to holders of record July 23, 2026.
-
Cumberland closes $100M sale of branded products to Apotex; retains ifetroban pipeline
Sold Acetadote, Caldolor, Kristalose, Sancuso, Vaprisol, Vibativ for $100M cash.
-
Shareholders approve sale of Cumberland's FDA-approved products to Apotex
Shareholders voted 10,492,455 For (99.84% of votes cast), 15,904 Against, 1,267 Abstain.
-
Cumberland Pharma enters $100M strategic transaction with Apotex, reports Q1 revenue $9.1M
Entered $100M cash deal to sell FDA-approved brand portfolio to Apotex Inc.; subject to shareholder approval and closing conditions.
-
Cumberland Pharma sells commercial products to Apotex for $100M, retains pipeline
Apotex acquires six FDA-approved brands (Acetadote, Caldolor, Kristalose, Sancuso, Vaprisol, Vibativ) for $100M cash.
-
Cumberland Pharma reports Q4 revenue up 31% to $13.7M; full-year adjusted earnings $1.7M
Full-year 2025 net revenue $44.5M (+18% YoY); net loss improved to $2.9M from $6.5M.
-
Cumberland Pharma gets FDA Fast Track for ifetroban in DMD heart disease
FDA Fast Track Designation granted for ifetroban targeting fatal heart disease in Duchenne muscular dystrophy.
-
Cumberland Pharma reports Q3 net loss of $1.9M; YTD revenue up 12% to $30.8M
Net revenue for Q3 2025 was $8.3M; YTD $30.8M (+12% vs. 2024).
-
Cumberland Pharmaceuticals forms joint venture with RedHill to commercialize Talicia H. pylori therapy
Cumberland and RedHill form new jointly owned company; Cumberland provides $4M in investment capital.
-
Cumberland Pharma reports Q2 revenue up 10% YoY; YTD revenue +23%
Q2 net revenue $10.8M (+10% YoY); YTD net revenue $22.6M (+23%).
-
Cumberland Q1 revenue $11.7M (+38% YoY), net profit $1.3M; DMD Phase II positive, Vibativ China OK
Net revenue $11.7M vs $8.5M prior year, 38% increase.
-
Cumberland's ifetroban shows 5.4% cardiac improvement in DMD Phase 2 trial
High-dose ifetroban improved LVEF by 3.3% vs. placebo and 5.4% vs. natural history controls.
-
Cumberland Pharma Q4 revenue +11.6% to $10.4M; full-year net loss $6.4M
Q4 2024 net revenue $10.4M, up 11.6% YoY; full-year revenue $38M.
-
Cumberland gets NMPA approval in China for Vibativ; exclusive deal with SciClone
Vibativ (telavancin) approved by China's NMPA for hospital-acquired pneumonia, ventilator-associated pneumonia, and complicated skin infections.
-
Cumberland Pharma Phase 2 ifetroban trial meets primary endpoint in DMD heart disease
High-dose ifetroban (300mg/day) produced 3.3% LVEF improvement vs placebo decline of 1.5%, net 4.8% benefit.
-
FDA approves simplified dosing regimen for Cumberland's Acetadote IV NAC
FDA approved sNDA for Acetadote on Dec 9, 2024; new regimen combines first two bags into a single slower infusion.
-
Cumberland Pharma Q3 net loss $1.5M; Caldolor study, DMD designations announced
Q3 2024 net revenue $9.1M; net loss $1.5M ($0.11 loss per share); adjusted loss $0.26M ($0.02 per share).
-
Cumberland announces study showing Caldolor reduces adverse drug reactions vs ketorolac
Study analyzed records of >17M patients; compared 31,046 Caldolor vs 124,184 ketorolac adults.
-
CMS denies Caldolor separate Medicare reimbursement under NOPAIN Act for CY2025
CMS excluded Caldolor from NOPAIN Act separate payment list announced Nov 1, 2024 for CY2025.
-
Cumberland Pharma Q2 revenue $9.9M, up 16% sequentially; adjusted earnings positive
Q2 net revenue $9.9M, 16% increase from Q1 2024; year-to-date $18.3M.
-
Cumberland Pharmaceuticals Q1 net loss $1.9M; revenue $8.5M
Net revenue $8.5M; Kristalose $3.2M, Sancuso $1.8M, Vibativ $1.6M, Caldolor $1.5M.
-
Cumberland Pharma reports 2023 net loss of $6.3M; revenue $40M; Caldolor labeling expanded to infants
Net loss $6.3M for 2023, includes $3.3M non-cash charge on product discontinuation; adjusted earnings $2.4M ($0.17/share).
-
Cumberland Pharma Q2 revenue $10.9M (+6% YoY); net income $0.9M
Q2 net revenue $10.9M (+6% vs prior year, +18% sequential); YTD revenue $20.1M.
-
Cumberland reports ifetroban well-tolerated with positive trend in DMD trial; no stat-sig
Interim analysis from 25 patients after 6 months; both ifetroban doses well-tolerated.
-
FDA approves Caldolor for infants aged 3-6 months; only injectable non-opioid for pain/fever in that age group
FDA approval expands Caldolor label to include infants 3 months to 6 months for pain and fever.
-
Cumberland Pharma Q1 net revenue $9.2M, adj. EPS $0.11; expects Caldolor Medicare boost under NOPAIN Act
Q1 2023 net revenues of $9.2M; net income of $0.2M ($0.01 EPS); adjusted earnings of $1.7M ($0.11 EPS).
-
Cumberland Pharma's Caldolor expected to qualify for separate Medicare reimbursement under NOPAIN Act from 2025
NOPAIN Act requires Medicare to provide separate reimbursement for non-opioid pain management products in outpatient hospital and ambulatory surgical center settings.
-
FDA grants barrier-to-innovation waiver; Cumberland to receive ~$1.9M refund for RediTrex fees
FDA reversed prior denial and granted barrier-to-innovation waiver on March 30, 2023, after reconsideration request.
-
Cumberland Pharma reports 17% revenue growth to $42M in FY2022; adj. EPS $0.14
FY2022 revenue $42.0M (+17% YoY); net loss $5.6M ($0.38/sh); adj. earnings $2.1M ($0.14/sh) vs adj. loss $1.2M in 2021.
-
Cumberland Q3 revenue up 41% to $11.4M; net loss narrows to $0.4M
Net revenue $11.4M vs $8.1M a year ago, driven by Sancuso ($4.0M) and Kristalose ($3.9M).