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ADMA Q2 2026 net income $37.8M (+11% YoY); ASCENIV revenue $102.9M (+24% YoY)
Total revenue $124.4M (+2% YoY); GAAP net income $37.8M (+11% YoY); GAAP basic EPS $0.17 (+17% YoY).
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ADMA Q1 revenue flat at $114.5M, ASCENIV up 28%; withdraws long-term guidance
Revenue $114.5M flat YoY; ASCENIV rev $97.5M (+28%) offset by BIVIGAM -54%.
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ADMA Biologics receives FDA approval to expand ASCENIV label to pediatric patients 2 years+
FDA approved label expansion for ASCENIV to include pediatric primary humoral immunodeficiency patients aged 2 years and older.
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ADMA Biologics refutes Culper Research short seller allegations; provides inventory & demand data
Demand for ASCENIV growing; end-user demand increased past two years; current days on hand average 90 days as of March 22, 2026.
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ADMA Biologics announces $125M accelerated share repurchase as part of $200M 2026 buyback plan
$125M ASR with JPMorgan; initial receipt of ~6.4M shares (~80% of expected) on March 3, 2026 at $15.57 close.
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ADMA Biologics reports record FY2025 revenue $510M (+20%), Adj. EBITDA $231M (+40%); CFO transition to Kohler
FY2025 total revenue $510.2M (+20% YoY); ASCENIV revenue $363M (+51% YoY). Gross margin 57.4% vs 51.5%.
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ADMA prelim FY2025 rev ~$510-511M, raises FY2026 rev/EBITDA guidance, targets >$1.1B by 2029
Preliminary FY2025 total revenue ~$510-511M, meeting or exceeding prior guidance. Cash grew to ~$88M with ~$40M Q4 operating cash flow.
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ADMA Q3 revenue $134.2M (+12% YoY); raises FY25 revenue guidance to $510M+, FY26 to $630M+
GAAP net income $36.4M (+1% YoY); adjusted EBITDA $58.7M (+29% YoY).
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ADMA Biologics Q2 revenue up 29% underlying; launches yield-enhanced IG mfg
Q2 2025 total revenue $122.0M, up 14% YoY (29% excluding $12.6M prior-year Medicaid reversal).
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ADMA Q1 revenue up 40% to $114.8M; raises FY2025/2026 guidance; authorizes $500M buyback
Q1 total revenue $114.8M (+40% YoY); GAAP net income $26.9M (+51% YoY); adjusted EBITDA $47.9M (+81% YoY).
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ADMA Biologics receives FDA approval for yield enhancement process; expects ~20% output increase
FDA approved innovative production yield enhancement process increasing yields by ~20% from same plasma volume.
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ADMA Biologics FY24 revenue $426.5M (+65% YoY); raises FY25/26 guidance
FY 2024 total revenue $426.5M (+65% YoY); GAAP net income $197.7M incl. $84.3M tax benefit; Adjusted EBITDA $164.6M (+309% YoY).
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ADMA prelim FY2024 rev $417-425M, guides FY2025 >$485M
FY2024 preliminary total revenue $417-425M, exceeding prior guidance of $415M; cash >$100M with $30M debt repaid in Q4.
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ADMA Biologics Q3 total revenue $119.8M (+78% YoY); GAAP net income $35.9M (+1,300%)
Revenue $119.8M (+78% YoY); GAAP net income $35.9M (+1,300%); Adj. EBITDA $45.4M (+256%)
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ADMA Biologics Q2 revenue $107.2M (+78% YoY); raises FY2024 revenue guidance to >$400M
Q2 2024 total revenue $107.2M, up 78% YoY; GAAP net income $32.1M vs loss of $6.4M a year ago.
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ADMA Biologics Q1 revenue $81.9M (+44% YoY); raises FY2024-25 guidance
GAAP net income $17.8M vs net loss of $6.8M in prior year; adjusted EBITDA $26.4M, a 970% increase.
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FDA approves extended room temperature storage for ADMA's ASCENIV and BIVIGAM
FDA approved supplemental BLAs to allow 4-week room temperature (25°C) storage at any time during the 36-month shelf life.
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ADMA Biologics Q4 rev $73.9M (+48%); FY rev $258.2M; raises FY24/25 guidance
Q4 2023 total revenue $73.9M, up 48% YoY; FY 2023 total revenue $258.2M, up 68% YoY.
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ADMA Biologics CFO Brian Lenz steps down; CEO Grossman named interim CFO
CFO Brian Lenz transitions to consulting role effective April 1, 2024; consulting agreement through March 31, 2025.
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ADMA raises FY2024-25 revenue guidance; preliminary Q4 rev $72-74M, FY rev $256-258M
Q4 2023 preliminary revenue $72-74M; full year $256-258M.
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ADMA Biologics refinances with $135M Ares facility, repays $159M Hayfin debt, reduces debt 15%
New $135M senior secured credit facility ($72.5M revolver + $62.5M term loan) fully drawn to repay prior Hayfin debt.
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FDA approves ADMA's BIVIGAM for pediatric PI patients aged 2 and older
FDA approved supplemental BLA for BIVIGAM to treat primary humoral immunodeficiency (PI) in patients 2 years and older.
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ADMA receives FDA approval for 10th plasma collection center; achieves plasma supply self-sufficiency
FDA approval for Laurel, MD facility (10th ADMA BioCenters center) to introduce source plasma into interstate commerce.
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ADMA Biologics Q3 2023: first-time net income $2.6M, revenue $67.3M (+64% YoY), raises FY guidance
Total revenues $67.3M, up 64% YoY; first-time positive GAAP net income of $2.6M (vs $14.9M loss YoY).
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ADMA Biologics raises FY2023 revenue guidance to >$240M; Q2 revenue up 77% to $60.1M
Q2 2023 total revenues $60.1M (+77% YoY); gross margin 27.8% (vs. 22.9% Q2 2022); normalized margin 31-32% excl. IT disruption.
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ADMA Biologics receives FDA approval for ninth plasma collection center in Dallas, GA
FDA approved Dallas, GA facility's BLA; center began plasma collection in Q3 2022.
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ADMA Biologics Q1 revenue $56.9M (+96% YoY); first-time positive Adjusted EBITDA $2.5M
Total revenues $56.9M, up 96% YoY; net loss narrowed to $6.8M from $25.0M.