NASDAQ$NVCT

Nuvectis Pharma Inc · Q4 2024 earnings

Q4 2024 earnings · · Before market open · Investor relations

Briefing

Reported financial results for the year ended December 31, 2024 and provided an update on recent business progress.

Nuvectis Pharma reported its full year 2024 financial results, highlighting progress in the development of its clinical-stage drug candidates NXP800 and NXP900, a follow-on offering providing $15.5 million in gross proceeds, and an extension of the company's cash runway into 2027.

  • NXP800 was granted Orphan Drug Designation by the U.S. FDA for the treatment of ARID1a-deficient cancers.
  • Enrollment is ongoing in the Phase 1b clinical trial for NXP800, with an update expected in the second quarter.
  • Enrollment continues in the Phase 1a dose escalation clinical trial for NXP900, with Phase 1b program preparations underway.
  • A follow-on offering provided Nuvectis with $15.5M in gross proceeds, extending the cash runway into 2027.

Headline financials

Total Revenue

$0.00

Previous: $0.00
EPS (adj)

-$0.36

Previous: -$0.41+12.2%
Capital Expenditures

$0.00

No prior period
Net Income

-$6.25M

Previous: -$6.62M+5.6%
Operating Income

-$6.45M

Previous: -$6.87M+6.1%
Gross Profit

$0.00

Previous: $0.00
R&D Expense

$4.5M

Previous: $4.27M+5.4%

Revenue & EPS history

Nuvectis Pharma · Revenue · Quarterly

$0

Q4 2024

Forward guidance

Nuvectis is well-positioned to generate meaningful results in its clinical portfolio in 2025 and beyond.

Tailwinds

  • Continued progress with the NXP800 and NXP900 programs
  • Strength and drug development expertise of our team
  • Expanded cash resources
  • NXP800 potential ability to become a therapeutic option for the treatment of platinum-resistant, ARID1a-mutated ovarian carcinoma, cholangiocarcinoma, and potentially other cancer indications
  • NXP900's therapeutic potential

Headwinds

  • Outcome of events are subject to inherent uncertainties, risks, assumptions, market and other conditions
  • Risks related to preclinical studies for NXP800 and NXP900
  • Risks related to the Phase 1a data for NXP800 and the NXP900 Phase 1a study data to date
  • Uncertainties regarding the potential ability of the 75mg/day dose intensity in the NXP800 Phase 1b study to generate satisfactory safety and efficacy results
  • Timing for completion of the clinical trials

Historical earnings impact

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

Avg. return before/after earnings

Based on 20 quarterly earnings reports · overlaid with Q4 2024

Historical avgQ4 2024

+2.4%

Avg return

Earnings day

+7.2%

Avg return

5 days after

-3.7%

Avg return

30 days after

65%

13 / 20 earnings

Positive

+29.2%

Q3 2024

Best reaction

-14.9%

Q1 2024

Worst reaction

Earnings price reactions
QuarterReport dateReaction (Day 0)+5 days+30 days
Q1 2026+9.4%+31.6%+8.8%
Q4 2026+0.5%+0.2%+3.3%
Q3 2025-7.9%-3.5%+6.1%
Q2 2025-5.4%-17.7%-10.6%
Q1 2025+6.4%+8.3%-9.4%
Q4 2024-5.8%-9.1%+31.1%
Q3 2024+29.2%+71.3%-24.6%
Q1 2024-14.9%-15.3%-13.6%
Q4 2023-4.5%-0.4%-25.1%
Q3 2023-7.9%-6.6%-8.4%
Q2 2023+1.4%+1.1%-7.0%
Q1 2023+5.8%+6.3%+14.0%
Q4 2022-7.1%-9.5%+9.2%
Q3 2021+0.9%-3.5%+7.7%
Q3 2022+0.9%-3.5%+7.7%
Q2 2021+1.1%+10.1%-0.6%
Q2 2022+2.6%-3.0%-3.7%
Q1 2021+18.8%+28.8%-24.4%
Q4 2021+18.8%+33.6%-15.6%
Q1 2022+5.4%+25.2%-19.4%

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