HIND Vyome Holdings, Inc

BEARISH Impact: 5/10 8-K
Horizon weeks Filed May 29, 2026 Processed 15d 3h ago SEC 0001213900-26-062458
8-K Item 2.02: Earnings release
Latest settled — T+5d
HIND ▼ -3.42% at T+5d
SHORT call ✓ call won +3.42% · α vs SPY +3.13% · entry $2.34 → $2.26
Next anchor: T+20d in 16d
Currently $2.30 · +1.71% from $2.34 entry (call sign-flipped)
Entry anchored
May 28, 03:59 PM ET
via Databento tick
T+1d
-0.85%
call +0.85% · α +1.13%
$2.32
settled 12d ago
T+5d
-3.42%
call +3.42% · α +3.13%
$2.26
settled 8d ago
T+20d
call — · α —
in 16d
T+60d
call — · α —
in 2mo

Price Chart

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Executive Summary

Vyome Holdings reported Q1 2026 EPS of -$0.15, beating the consensus estimate of -$0.19 by 21%, but revenue collapsed 84% YoY to $31.6K from $198.6K. The company highlighted FDA filings for Orphan Drug Designation on VT-1953, an in-licensing deal for JAK inhibitors with Impetis Biosciences (TATA Enterprise), and a $5.29M equity raise at a 59% premium — but the revenue decline and cash burn dominate the outlook for a $16M market-cap clinical-stage biotech.

Key Financial Metrics

Gross Margin
52.7%

Actionable Insight

The EPS beat is mechanical on a tiny base and irrelevant for a clinical-stage biotech. The key catalysts are FDA feedback on VT-1953 Orphan Drug Designation and whether the JAK inhibitor in-license progresses to clinical milestones. With only $8.8M cash and $1.1M quarterly burn, watch for warrant exercise or future dilutive offerings if pipeline milestones slip. The revenue collapse is not material for the thesis — pipeline milestones are the only driver for HIND.

Key Facts

  • Revenue fell 84% YoY to $31.6K (Q1 2026) from $198.6K (Q1 2025), though revenue remains immaterial for a clinical-stage biotech
  • EPS of -$0.15 beat consensus of -$0.19 by 21.1%
  • Net loss widened to -$985.5K from -$294.0K YoY, driven by operating expenses tripling to $1.15M
  • Cash & equivalents: $8.8M as of March 31, 2026, up from $5.0M at Dec 2025 after a $5.29M equity raise
  • Filed Orphan Drug Designation application with FDA for VT-1953 and in-licensed two JAK inhibitor assets from Impetis Biosciences (TATA) with payments at commercialization
  • Clean capital structure maintained — no debt, preferred, or toxic instruments

Financial Impact

Revenue declined ~84% YoY to $31.6K; net loss widened to -$985.5K; cash burn rate of ~$1.1M/quarter ($8.8M cash = ~8 quarters runway)

revenuenet_losscash_positionoperating_expenses

Risk Factors

  • VT-1953 Orphan Drug Designation may be denied or delayed
  • Cash runway extends only through ~8 quarters at current burn; clinical setbacks would force dilutive financing
  • Revenue disappearance to $31.6K reduces credibility of any near-term commercialization revenue
  • Post-market close May 28 — elevated after-hours volatility risk

Market Snapshot

Exchange
Nasdaq
Sector
Pharmaceutical Preparations
Analyst Consensus
86% bullish (7 analysts)

Documents Analyzed

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

DocumentAccession Number
8-K Filing (Primary)0001213900-26-062458
Document: ea0292643-8k_vyome.htm0001213900-26-062458
Document: 0001213900-26-062458-index-headers.html0001213900-26-062458
Document: 0001213900-26-062458-index.html0001213900-26-062458
Document: 0001213900-26-062458.txt0001213900-26-062458
8-K Data (Synthetic)0001213900-26-062458
2 reports for HIND
Performance horizon

Track record builds as more directional reports settle.

Filters
Rows
Reports for HIND — sortable, filterable
Type Now
May 29, 2026
15d ago
8-K
BEARISH ★ 5/10
$2.34 $2.26▲ +3.42%▲ +3.13%$2.30 (+1.71%)
Feb 25, 2026
15w ago
8-K
BULLISH ★ 8/10
$3.36 $2.91▼ −13.39%▼ −12.27%$2.30 (−31.55%)
Showing 2 of 2

US Market Status

Market Closed — Opens Mon (45h 28m)

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