8-K ·Filed Aug 10, 2026

PROK

PROKIDNEY CORP.
NEUTRAL
Impact 5/10
Horizonmonths Processed1mo ago SEC0001193125-26-342397
8-K Item 2.02: Earnings release
Actionable Insight • Neutral

The stock will trade on PROACT 1 enrollment completion and the Q2 2027 topline readout timeline, not on quarterly financials. Monitor for any updates on the confirmatory full enrollment (~470 patients) expected in H2 2026 and any regulatory interactions that could derisk the accelerated approval pathway.

DirectionNeutral
Confidencehigh
Horizonmonths
Latest settled — T+20d ⚠ clustered
PROK ▲ +14.91% at T+20d
NEUTRAL call ✓ call won +14.91% · α vs SPY +15.97% · entry $1.61 → $1.85
Next anchor: T+60d in 5w
Latest observation: T+34 +11.53% FF3 residual α
Entry anchored
Aug 10, 04:05 PM ET
via 1-min bar
T+1d
-8.07%
call -8.07% · α -8.32%
$1.48
settled 7w ago
T+5d
-14.29%
call -14.29% · α -13.88%
$1.38
settled 7w ago
T+20d
+14.91%
call +14.91% · α +15.97%
$1.85
settled 24d ago
T+60d
—
call — · α —
—
in 5w

Price Chart

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Executive Summary

ProKidney reported Q2 2026 results with no revenue or EPS surprises vs consensus, as the company remains a pre-commercial clinical-stage biotech. The key catalyst is the completion of enrollment for the PROACT 1 accelerated approval analysis (~320 patients), positioning the company for pivotal eGFR slope topline results in Q2 2027. Cash burn continues with $181.6M in cash supporting operations into mid-2027, and the net loss widened to $46.4M from $37.0M YoY.

Key Financial Metrics

EPS
$-0.15
est $-0.13 · -15.4%
Revenue
$150.0K
est $149.0K · +0.7% · -32.1% YoY
Rating
in line

Key Facts

  • Completed enrollment of ~320 patients for the PROACT 1 accelerated approval efficacy analysis; pivotal topline results expected Q2 2027
  • Cash, cash equivalents and marketable securities totaled $181.6M as of June 30, 2026, down from $224.9M at March 31, 2026
  • Net loss before noncontrolling interest was $46.4M for Q2 2026 vs $37.0M for Q2 2025
  • R&D expenses increased to $36.1M from $25.9M YoY, driven by PROACT 1 clinical costs
  • Appointed Kenneth Locke as Chief Technical Officer in June 2026

Financial Impact

No revenue or EPS surprise; cash burn of ~$43M per quarter; cash runway into mid-2027

cashnet lossR&D expenses

Risk Factors

  • Clinical trial failure or negative eGFR slope results in Q2 2027
  • Cash runway only into mid-2027, requiring future dilutive financing
  • Regulatory risk: FDA may require additional studies before BLA acceptance

Market Snapshot

Exchange
Nasdaq
Sector
Biological Products, (No Diagnostic Substances)
Analyst Consensus
67% bullish (15 analysts)

Investment Themes

Biotech & Drug Discovery

Documents Analyzed

This report is based on 6 SEC documents filed with EDGAR.

DocumentAccession Number
8-K Filing (Primary)0001193125-26-342397
Document: prok-20260810.htm0001193125-26-342397
Document: 0001193125-26-342397-index-headers.html0001193125-26-342397
Document: 0001193125-26-342397-index.html0001193125-26-342397
Document: 0001193125-26-342397.txt0001193125-26-342397
8-K Data (Synthetic)0001193125-26-342397
6 reports for PROK
Performance horizon
Filters
Rows
Reports for PROK — sortable, filterable
TypeNow
Aug 10, 2026
7w ago
8-K
NEUTRAL ★ 5/10
$1.61 $1.85▲ +14.91%▲ +15.97%$1.72 (+6.83%)
Aug 10, 2026
7w ago
Press Release
NEUTRAL ★ 5/10
$1.61 $1.85▲ +14.91%▲ +15.97%$1.72 (+6.83%)
May 15, 2026
20w ago
8-K
NEUTRAL ★ 4/10
$1.66 $1.67▲ +0.60%▼ −1.52%$1.72 (+3.61%)
May 15, 2026
20w ago
Press Release
NEUTRAL ★ 5/10
$1.66 $1.67▲ +0.60%▼ −1.52%$1.72 (+3.61%)
Apr 17, 2026
24w ago
DEFA14A
NEUTRAL ★ 2/10
$2.10 $1.61▼ −23.33%▼ −27.54%$1.72 (−18.10%)
Mar 18, 2026
28w ago
Press Release
MIXED ★ 6/10
$1.95 $2.18▲ +11.79%▲ +4.17%$1.72 (−11.79%)
Showing 6 of 6

US Market Status

Market Closed — Opens Mon (65h 8m)

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