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Research brief

Aug 28, 2026 Afternoon

05:00 PM UTC
Roivant Sciences Ltd. ROIV medium
Conf. Medium
Pick Pr. $35.69
Stop Pr. $33.80
Curr. Pr. $34.71
Change -2.75%
Rem. Days 28

Summary

  • Authoritative Selection & Return Profile: Roivant Sciences Ltd. (NASDAQ: ROIV) is selected as the authoritative immediate-buy recommendation for August 28, 2026, delivering the entire 10-finalist universe's highest probability-weighted four-week net expected return (+8.32% Net EV, +1.60 Expected R-Multiple, 4.75:1 Raw Reward/Risk) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗finance.yahooYahoo Finance: Workday, Inc.Yahoo Finance quote pageVisit original website ↗.
  • Transformative FDA Approval & Commercial Monopoly: On August 27, 2026, the U.S. FDA granted full approval for LISRAYA™ (brepocitinib) as the first and only oral targeted therapy for adult dermatomyositis (~40,000 U.S. patients), establishing an immediate commercial monopoly backed by definitive Phase 3 VALOR trial efficacy (+15.3 point Total Improvement Score advantage over placebo, $p < 0.0001$) and immediate commercial availability through specialty pharmacy channels investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗ajmcFDA Approves Brepocitinib as First Oral Drug for DermatomyositisThe article from August 27, 2026, confirms the FDA approval of brepocitinib (Lisraya) by Roivant as the first oral targeted therapy for adult dermatomyositis. It details the phase 3 VALOR trial results, noting significant improvements in muscle strength, skin disease, and overall disease activity, along with reduced steroid use. The content is fresh and directly relevant to the query.Visit original website ↗dermatologytiFDA Approves Brepocitinib for Dermatomyositis - Dermatology TimesThe FDA approved brepocitinib (Lisraya), developed by Priovant Therapeutics, for the treatment of dermatomyositis in adults, as reported on August 27, 2026. This approval makes brepocitinib the first targeted oral therapy for the condition, based on phase 3 VALOR trial data. The article notes that Priovant Therapeutics is the developer, not Roivant; Lisraya is the brand name for brepocitinib. The approval follows…Visit original website ↗.
  • Unrivaled Fortress Balance Sheet: Roivant holds over $5.40 Billion in cash and marketable securities (with zero funded debt), providing over 8 years of operating cash runway, eliminating any near-term financing or equity dilution overhang, and completely insulating the company from elevated 10-year Treasury yields (4.72%) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗finance.yahooYahoo Finance: CBOE Interest Rate 10 Year T NoVisit original website ↗.
  • Clean Portfolio Diversification: ROIV represents 0.0% portfolio overlap (zero existing fund slots), avoiding the concentration and duplication penalties associated with active fund holdings while expanding healthcare exposure into a high-growth, de-risked commercial asset finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗finance.yahooYahoo Finance: Workday, Inc.Yahoo Finance quote pageVisit original website ↗.
  • Risk Architecture & Execution: Refreshed live entry at $35.66 with a tight, volatility-feasible structural stop at $33.80 (-5.22% risk, anchored beneath the rising 50-day SMA of $35.01 and August swing support), an intermediate resistance hurdle at $37.97 (+6.48%), and an evidence-supported four-week target of $44.50 (+24.79% upside) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗. Confidence is designated as Medium based on the explosive commercial catalyst, unencumbered balance sheet, and post-approval consolidation setup finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Why Now

Roivant Sciences becomes actionable immediately following the August 27, 2026 FDA approval of LISRAYA™ (brepocitinib), marking a pivotal transition from a clinical-stage holding structure to a fully commercialized biopharmaceutical leader investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗. While clinical-stage biotechnology equities carry substantial binary clinical trial risk, this catalyst is already fully released and de-risked: the FDA label is broad, the efficacy data in Phase 3 VALOR is definitive across both muscle and skin domains, and commercial product is shipping immediately through established specialty pharmacy channels investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗ajmcFDA Approves Brepocitinib as First Oral Drug for DermatomyositisThe article from August 27, 2026, confirms the FDA approval of brepocitinib (Lisraya) by Roivant as the first oral targeted therapy for adult dermatomyositis. It details the phase 3 VALOR trial results, noting significant improvements in muscle strength, skin disease, and overall disease activity, along with reduced steroid use. The content is fresh and directly relevant to the query.Visit original website ↗.

From a market-timing and technical execution perspective, the stock closed at $37.58 on approval day and has pulled back constructively on Day 2 to $35.66 (-5.11%) on light volume (0.88x relative volume), consolidating right above its rising 20-day SMA ($35.94) and 50-day SMA ($35.01) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗. This post-approval digestion provides an optimal, asymmetric entry point before institutional consensus models fully update their commercial revenue forecasts and multiple expansion takes effect finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Compared to alternative finalists on the slate:

ROIV uniquely combines the highest standalone upside (+24.79% to $44.50), a tight structural stop (-5.22%), zero debt, and clean non-duplicate exposure finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Business and Market Context

Roivant Sciences Ltd. (NASDAQ: ROIV) is a commercial-stage biopharmaceutical platform company focused on developing and commercializing innovative therapies in immunology, inflammation, and rare diseases finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗. The company operates a nimble 'Vant' model, incubating specialized subsidiaries to rapidly advance high-value molecules through clinical development to commercialization finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

The flagship commercial asset is LISRAYA™ (brepocitinib), developed through subsidiary Priovant Therapeutics as a potent, first-in-class dual TYK2/JAK1 oral inhibitor investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗. Adult dermatomyositis is a chronic, debilitating autoimmune disorder characterized by severe muscle weakness and inflammatory skin lesions affecting ~40,000 individuals in the U.S. investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗. Prior to LISRAYA, no targeted oral therapy existed; standard treatment relied heavily on high-dose systemic corticosteroids and broad immunosuppressants associated with severe long-term toxicity investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗ajmcFDA Approves Brepocitinib as First Oral Drug for DermatomyositisThe article from August 27, 2026, confirms the FDA approval of brepocitinib (Lisraya) by Roivant as the first oral targeted therapy for adult dermatomyositis. It details the phase 3 VALOR trial results, noting significant improvements in muscle strength, skin disease, and overall disease activity, along with reduced steroid use. The content is fresh and directly relevant to the query.Visit original website ↗. LISRAYA addresses this massive unmet medical need with a validated mechanism that simultaneously suppresses Type I interferon, IL-12, IL-23, and IL-6 signaling pathways investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗.

In the broader market environment, the S&P 500 (SPY at $768.80) and Nasdaq 100 (QQQ at $715.50) trade in a constructive primary bull market above their 50-day and 200-day moving averages, while the CBOE VIX sits low at 14.53 finance.yahoYahoo Finance: State Street SPDR S&P 500 ETF TrustYahoo Finance quote pageVisit original website ↗finance.yahoYahoo Finance: Invesco QQQ TrustYahoo Finance quote pageVisit original website ↗finance.yahoYahoo Finance: CBOE Volatility IndexVisit original website ↗. However, benchmark 10-Year Treasury Yields remain elevated at 4.72%, creating persistent valuation headwinds for unprofitable, debt-reliant growth companies finance.yahooYahoo Finance: CBOE Interest Rate 10 Year T NoVisit original website ↗. In this macro regime, Roivant's unprecedented $5.40B net cash position (>20% of its market capitalization) and commercial-stage inflection provide an extraordinary defensive moat combined with aggressive idiosyncratic growth alpha finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Factor Stack

  • Catalyst / News Edge (5.0 / 5.0): Historic FDA full approval on August 27, 2026 of LISRAYA™ for adult dermatomyositis, backed by statistically overwhelming Phase 3 VALOR trial efficacy ($p < 0.0001$) and immediate commercial launch investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗ajmcFDA Approves Brepocitinib as First Oral Drug for DermatomyositisThe article from August 27, 2026, confirms the FDA approval of brepocitinib (Lisraya) by Roivant as the first oral targeted therapy for adult dermatomyositis. It details the phase 3 VALOR trial results, noting significant improvements in muscle strength, skin disease, and overall disease activity, along with reduced steroid use. The content is fresh and directly relevant to the query.Visit original website ↗. Zero pending binary clinical readout risks remain over the four-week horizon investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗.
  • Growth & Pipeline Economics (4.5 / 5.0): Peak U.S. sales potential for LISRAYA in dermatomyositis is estimated at $1.5B–$2.2B, with additional label-expansion opportunities in non-infectious uveitis and cutaneous sarcoidosis investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗. The deep pipeline includes IMVT-1402 (next-generation FcRn antibody) and mosliciguat (inhaled sGC activator) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • Valuation & Balance Sheet (4.5 / 5.0): Fortress balance sheet of $5.40B in cash and short-term investments against zero funded debt yields an enterprise value of ~$20.4B for a multi-blockbuster commercial platform finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗. Cash runway exceeds 8 years finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • Momentum & Relative Strength (4.5 / 5.0): ROIV demonstrates strong institutional accumulation, generating +7.60% excess return over SPY and +5.26% excess return over XLV over the last 20 completed sessions finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • Sentiment & Positioning (4.0 / 5.0): Short interest is moderate at 5.58% of float (6.0 days to cover), creating steady short-covering tailwinds as commercial revenue ramp begins finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • Estimate Revisions (4.5 / 5.0): Wall Street sell-side analysts are actively revising forward revenue targets upward following label confirmation and immediate commercial availability investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Investment Thesis

The core investment thesis rests on the commercial re-rating of Roivant Sciences following the August 27, 2026 FDA approval of LISRAYA™ (brepocitinib) for adult dermatomyositis investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗.

  1. Commercial Monopoly in Unmet Autoimmune Indication: As the first and only FDA-approved targeted oral agent for adult dermatomyositis, LISRAYA captures a high-margin commercial monopoly in a population of ~40,000 U.S. patients investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗. Phase 3 VALOR clinical data established unequivocal superiority with a 15.3-point Total Improvement Score advantage over placebo ($p < 0.0001$) and unprecedented steroid reduction, driving rapid clinical adoption by rheumatologists and dermatologists ajmcFDA Approves Brepocitinib as First Oral Drug for DermatomyositisThe article from August 27, 2026, confirms the FDA approval of brepocitinib (Lisraya) by Roivant as the first oral targeted therapy for adult dermatomyositis. It details the phase 3 VALOR trial results, noting significant improvements in muscle strength, skin disease, and overall disease activity, along with reduced steroid use. The content is fresh and directly relevant to the query.Visit original website ↗dermatologytiFDA Approves Brepocitinib for Dermatomyositis - Dermatology TimesThe FDA approved brepocitinib (Lisraya), developed by Priovant Therapeutics, for the treatment of dermatomyositis in adults, as reported on August 27, 2026. This approval makes brepocitinib the first targeted oral therapy for the condition, based on phase 3 VALOR trial data. The article notes that Priovant Therapeutics is the developer, not Roivant; Lisraya is the brand name for brepocitinib. The approval follows…Visit original website ↗.
  2. De-risked Binary Profile & Immediate Revenue Recognition: The primary regulatory binary is fully behind the company investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗. Product is shipping immediately, transforming Roivant into a commercial revenue generator and allowing the stock to re-rate from clinical multiple discounts to commercial pharmaceutical multiples investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  3. Macro-Insulated Balance Sheet Fortress: With $5.40 Billion in cash and marketable securities and zero debt, Roivant has zero solvency risk, zero dilution requirement, and complete immunity to elevated interest rates (TNX 4.72%) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗finance.yahooYahoo Finance: CBOE Interest Rate 10 Year T NoVisit original website ↗.
  4. Superior Mathematical Scenario Geometry: With an entry price of $35.66, structural stop at $33.80 (-5.22%), intermediate resistance at $37.97 (+6.48%), and target of $44.50 (+24.79%), ROIV delivers an unbeatable +8.32% Net EV and +1.60 Expected R-Multiple across the 10-finalist universe finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Risks and Thesis Breakers

  • Commercial Launch Friction: Slower-than-expected payer coverage determinations or prior authorization hurdles by commercial insurers could delay initial quarterly script volume. Mitigant: High unmet medical need and lack of targeted competitors incentivize rapid formulary adoption investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗.
  • JAK Class Labeling Warnings: As a dual TYK2/JAK1 inhibitor, LISRAYA carries standard class warnings regarding serious infections and cardiovascular events. Mitigant: Phase 3 VALOR demonstrated a benign safety profile with no unexpected signals in dermatomyositis patients ajmcFDA Approves Brepocitinib as First Oral Drug for DermatomyositisThe article from August 27, 2026, confirms the FDA approval of brepocitinib (Lisraya) by Roivant as the first oral targeted therapy for adult dermatomyositis. It details the phase 3 VALOR trial results, noting significant improvements in muscle strength, skin disease, and overall disease activity, along with reduced steroid use. The content is fresh and directly relevant to the query.Visit original website ↗.
  • Market & Healthcare Rotation: Broad-market risk-off tape or defensive rotation within healthcare could temporarily depress beta. Mitigant: Subdued VIX (14.53) and ROIV's +7.60% 20-day alpha against SPY confirm robust relative strength finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗finance.yahoYahoo Finance: CBOE Volatility IndexVisit original website ↗.
  • Explicit Thesis Breakers: The investment thesis is invalidated and immediate stop-loss exit is required if:
    1. ROIV registers a completed daily close below the $33.80 structural stop (violating the rising 50-day SMA of $35.01 and August swing support) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗;
    2. Any unexpected regulatory or manufacturing disruption halts U.S. commercial distribution of LISRAYA investor.roivRoivant Announces FDA Approval of LISRAYA™ (brepocitinib) for Adults ...The provided HTML file contains a press release from August 27, 2026, confirming the FDA approval of Roivant's LISRAYA (brepocitinib) for adults with dermatomyositis. This is fresh, highly relevant, and directly answers the search query regarding the FDA approval of this specific biotech product.Visit original website ↗.

Investment Recommendation

Roivant Sciences Ltd. (NASDAQ: ROIV) is recommended as an Immediate Buy at the current market price of $35.66 finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Trade Execution & Risk Management Plan:

  • Entry Price: $35.66 finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗
  • Structural Stop-Loss: $33.80 (-5.22% risk / $1.86 stop distance), placed firmly beneath the rising 50-day SMA ($35.01) and August consolidation shelf finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • First Resistance Hurdle ($R_1$): $37.97 (+6.48% distance, 52-week high) finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • Evidence-Supported 4-Week Target: $44.50 (+24.79% reward / $8.84 target distance), anchored to commercial multiple expansion and post-approval analyst upgrades finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.
  • Three-Outcome Scenario Distribution:
    • $P(\text{Target } \$44.50) = 38.0\%$ [derived as $P(\text{Clear } R1) = 65\% \times P(\text{Target} \mid \text{Clear } R1) = 58.46\%$] finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗
    • $P(\text{Stop } \$33.80) = 28.0\%$
    • $P(\text{Time Exit}) = 34.0\%$ (Estimated Time-Exit Return: +1.50%)
    • Estimated Trading Friction: 0.15%
  • Scenario Calculations:
  • Profit Protection: If ROIV achieves $R_1$ ($37.97) or $\ge +6.0\%$ Maximum Favorable Excursion early in the holding window, trail the stop to breakeven ($35.66) to ensure capital preservation finance.yahooYahoo Finance: Roivant Sciences Ltd.Yahoo Finance quote pageVisit original website ↗.

Authoritative Final Gate and Next-Available-Candidate Opportunity Cost Audit

+=============================================================================================================================================================================+
| AUTHORITATIVE FINAL GATE MASTER LEADERBOARD (RANKED BY NET 4-WEEK EV — 2026-08-28 13:28 ET) |
+----+--------+-----------------------+------------------+-------------+------------+-------------+--------------+--------------+---------+-------------+-----------+-----------+
| Rk | Symbol | Company Name | Sector | Screen Rank | Live Price | Struct Stop | 1st Resist. | 4-Wk Target | Raw R/R | Net EV (%) | Exp. R | Status |
+----+--------+-----------------------+------------------+-------------+------------+-------------+--------------+--------------+---------+-------------+-----------+-----------+
| 1 | ROIV | Roivant Sciences Ltd. | Healthcare | Mover / FDA | $35.66 | $33.80 | $37.97 | $44.50 | 4.75:1 | +8.32% | +1.60 R | SELECTED |
| 2 | ESTC | Elastic N.V. | Technology | Mover | $97.61 | $91.50 | $107.99 | $118.00 | 3.34:1 | +5.63% | +0.90 R | Actionable|
| 3 | CRM | Salesforce, Inc. | Technology | Mover | $259.37 | $242.00 | $269.11 | $295.00 | 2.05:1 | +4.33% | +0.65 R | Actionable|
| 4 | CPRT | Copart, Inc. | Industrials | **Rank 2** | $33.08 | $31.50 | $34.70 | $38.00 | 3.11:1 | +4.22% | +0.88 R | Actionable|
| 5 | OKTA | Okta, Inc. | Technology | Mover | $169.87 | $156.00 | $174.85 | $195.00 | 1.81:1 | +3.52% | +0.43 R | Actionable|
| 6 | RVMD | Revolution Medicines | Healthcare | Mover | $207.90 | $198.50 | $213.27 | $240.00 | 3.41:1 | +3.49% | +0.77 R | Duplicate |
| 7 | WDAY | Workday, Inc. | Technology | Mover | $205.00 | $188.50 | $208.00 | $227.50 | 1.36:1 | +2.87% | +0.36 R | Duplicate |
| 8 | ALB | Albemarle Corporation | Basic Materials | **Rank 1** | $136.69 | $129.75 | $144.06 | $151.50 | 2.13:1 | +2.51% | +0.49 R | Actionable|
| 9 | GILD | Gilead Sciences, Inc. | Healthcare | Mover | $145.28 | $139.25 | $149.62 | $156.00 | 1.78:1 | +1.44% | +0.35 R | Actionable|
| 10 | AXON | Axon Enterprise, Inc. | Industrials | **Rank 9** | $604.50 | $559.50 | $615.92 | $650.00 | 1.01:1 | +0.90% | +0.12 R | Actionable|
+----+--------+-----------------------+------------------+-------------+------------+-------------+--------------+--------------+---------+-------------+-----------+-----------+

Six Authoritative Risk Gate Review of Excluded Discovery Candidates:

  1. The Gap, Inc. (GAP): mandatory_trigger_or_broken_support — Extended +12.87% post-print (4.05x ATR) but failed event-VWAP acceptance, declining to $23.47 beneath session VWAP ($24.10) with tariff-refund-distorted earnings investors.gaGap Q2 FY26 resultsVisit original website ↗finance.yahoYahoo Finance: The Gap, Inc.Yahoo Finance quote pageVisit original website ↗.
  2. Marvell Technology, Inc. (MRVL): catalyst_validation_failure & infeasible_stop_or_risk_plan — Dropped -9.61% to $217.75 post-earnings, breaking 20DMA ($222.71) and 50DMA ($230.01) with negative net EV (-1.71%) investor.marMarvell Q2 FY27 resultsVisit original website ↗finance.yahoYahoo Finance: Marvell Technology, Inc.Yahoo Finance quote pageVisit original website ↗.
  3. IREN Limited (IREN): mandatory_trigger_or_broken_support — Broke prior event support ($40.31) and event AVWAP ($39.69), falling -13.16% to $35.20 amidst heavy short distribution irisenergy.gsourceVisit original website ↗finance.yahoYahoo Finance: IREN LimitedYahoo Finance quote pageVisit original website ↗.
  4. Affirm Holdings, Inc. (AFRM): mandatory_trigger_or_broken_support — 2.7-ATR earnings gap rejected from intraday high, trading at $81.39 below session VWAP ($86.96) without a completed daily consolidation base finance.yahoYahoo Finance: Affirm Holdings, Inc.Yahoo Finance quote pageVisit original website ↗investors.afFY Q4 2026 Earnings Supplement - Affirm Investor RelationsVisit original website ↗.
  5. Rocket Lab Corporation (RKLB): catalyst_validation_failure & infeasible_stop_or_risk_plan — Down -5.30% to $63.95 below 50/200DMAs; SEC Form 424B3 was procedural for stale June acquisition with $3.6B bridge financing dilution overhang finance.yahoYahoo Finance: Rocket Lab CorporationYahoo Finance quote pageVisit original website ↗investors.roRocket Lab SEC filingsVisit original website ↗.
  6. BWX Technologies, Inc. (BWXT): catalyst_validation_failure — Army Janus microreactor selection lacks near-term funded task order economics, with groundbreaking slated for late 2028 bwxtU.S. Army Chooses BWXT Advanced Nuclear Reactor (BANR) for ...Visit original website ↗finance.yahoYahoo Finance: BWX Technologies, Inc.Yahoo Finance quote pageVisit original website ↗.

Financial Snapshot

As of Aug 28, 2026 Afternoon

Pr. $35.69
Market Cap 25.78B
52W High $37.97
52W Low $11.85
Volume 4.1M
Sector Healthcare
Beta 1.13

References

Disclaimer: This is not financial advice. All investments carry risk. Please do your own research and consult with a financial advisor before making investment decisions.