NASDAQ$HUMA

Humacyte Inc · Q1 2023 earnings

Q1 2023 earnings · · Investor relations

Briefing

Announced first quarter 2023 financial results and business update.

Humacyte reported its Q1 2023 financial results, highlighting the second RMAT designation by the FDA for Vascular Trauma and the completion of enrollment in the Phase 3 trial of HAV in Hemodialysis Access in End-Stage Renal Disease Patients. The company's net loss increased due to a change in the fair value of the contingent earnout liability.

  • Received second RMAT designation from the FDA for HAV in vascular trauma, potentially expediting BLA review.
  • Completed enrollment in Phase 3 trial of HAV in Hemodialysis Access, with top-line results expected in 2024.
  • Published data in The Lancet Regional Health - Europe highlighting successful HAV use in treating vascular trauma in Ukraine.
  • Announced collaboration with JDRF International to advance the development of the Biovascular Pancreas (BVP) product candidate for Type 1 diabetes.

Headline financials

Total Revenue

$0.00

Previous: $233K-100.0%
EPS (adj)

-$0.36

Previous: -$0.19-89.5%
Capital Expenditures

$1.15M

Previous: $22K+5136.4%
Free Cash Flow

-$19.8M

Previous: -$18.8M-5.2%
Net Income

-$37M

Previous: -$19.8M-86.6%
Operating Income

-$22.5M

Previous: -$21.8M-3.4%
Cash & Equivalents

$130M

Previous: $198M-34.6%
Total Assets

$183M

Previous: $264M-30.8%
Stock-Based Comp

$1.81M

Previous: $1.55M+16.9%

Revenue & EPS history

Humacyte · Revenue · Quarterly

$0

Q1 2023-100%vs Q1 2022
Beat estimate in 2 of 15 quarters(13%)
ActualEstimate

Forward guidance

Humacyte believes that its cash, cash equivalents short-term investments and planned funding from the Oberland funding agreement are adequate to fund operations past the anticipated timelines for potential approval and commercialization of the HAV in vascular trauma.

Tailwinds

  • Progress toward planned BLA filing of HAV in vascular trauma
  • Granted FDA’s Regenerative Medicine Advanced Therapy (RMAT) designation for the HAV
  • RMAT designation allows for more interactions with the FDA and expedited development and review of regenerative medicine products within the U.S.
  • Completed enrollment of a Phase 3 trial in hemodialysis access
  • Collaboration with JDRF International to advance the development of Humacyte’s BVP product candidate

Headwinds

  • Changes in applicable laws or regulations
  • Humacyte may be adversely affected by other economic, business, and/or competitive factors
  • The possibility of not receiving the necessary regulatory approvals for our products
  • The outcome of ongoing discussions with the FDA concerning the design of our ongoing V005 Phase 2/3 clinical trial
  • Uncertainties regarding the timing, scope, and rate of reimbursement for our HAVs

Historical earnings impact

How earnings announcements have historically affected this stock's price.

Avg. return before/after earnings

Based on 19 quarterly earnings reports · overlaid with Q1 2023

Historical avgQ1 2023

+5.1%

Avg return

Earnings day

+2.0%

Avg return

5 days after

+3.5%

Avg return

30 days after

62%

13 / 21 earnings

Positive

+37.0%

Q2 2023

Best reaction

-30.1%

Q2 2025

Worst reaction

Earnings price reactions
QuarterReport dateReaction (Day 0)+5 days+30 days
Q1 2026+22.9%-1.5%+15.2%
Q4 2025-15.1%-25.1%-33.0%
Q3 2025-3.2%-11.7%+2.3%
Q2 2025-30.1%-24.2%-40.3%
Q1 2025+19.5%+23.8%+25.4%
Q4 2024-2.5%-27.4%-28.4%
Q3 2024+4.9%+1.5%-8.2%
Q1 2024+21.2%+43.1%+60.8%
Q4 2023-12.8%-13.9%+2.8%
Q3 2023+7.3%+9.1%+27.9%
Q2 2023+37.0%+8.9%+19.0%
Q1 2023-6.1%-2.5%+1.1%
Q4 2022+4.9%-1.3%+7.1%
Q3 2022+2.2%-5.4%-4.5%
Q2 2022+8.6%+9.1%+2.5%
Q1 2022-9.5%-12.7%-18.8%
Q4 2021+14.1%+12.2%+16.5%
Q2 2021+14.1%+12.2%+16.5%
Q3 2021+9.0%+18.4%+4.0%
Q1 2021+0.0%+0.0%+4.9%
Q4 2020+21.2%+28.4%+1.5%
Q3 2020

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