® Developing Breakthrough Biologics, Life-changing Medicines Corporate Update September 2019 Legal Notices The information in this slide deck is current as of August 31, 2019, unless otherwise noted, and is qualified in its entirety by reference to MacroGenics’ Annual, Quarterly and Current Reports filed with the SEC. MacroGenics undertakes no obligation to update any of the information herein. Cautionary Note on Forward-Looking Statements Any statements in these materials about future expectations, plans and prospects for MacroGenics (“Company”), including statements about the Company’s strategy, future operations, clinical development of the Company’s therapeutic candidates, milestone or opt-in payments from the Company’s collaborators, the Company’s anticipated milestones and future expectations and plans and prospects for the Company and other statements containing the words “subject to”, "believe", “anticipate”, “plan”, “expect”, “intend”, “estimate”, “project”, “may”, “will”, “should”, “would”, “could”, “can”, the negatives thereof, variations thereon and similar expressions, or by discussions of strategy constitute forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including: the uncertainties inherent in the initiation and enrollment of future clinical trials, expectations of expanding ongoing clinical trials, availability and timing of data from ongoing clinical trials, expectations for regulatory approvals, other matters that could affect the availability or commercial potential of the Company's product candidates and other risks described in the Company’s filings with the Securities and Exchange Commission. In addition, the forward- looking statements included in this presentation represent the Company's views only as of the date hereof. The Company anticipates that subsequent events and developments will cause the Company's views to change. However, while the Company may elect to update these forward- looking statements at some point in the future, the Company specifically disclaims any obligation to do so, except as may be required by law. These forward-looking statements should not be relied upon as representing the Company’s views as of any date subsequent to the date hereof. Trademarks DART, TRIDENT, MacroGenics, the MacroGenics logo and “Breakthrough Biologics, Life-Changing Medicines” are trademarks or registered trademarks of MacroGenics, Inc. The Incyte logo is a registered trademark of Incyte Corporation. Investigational Agents All Company product candidates described or mentioned herein are investigational and have not yet been approved for marketing by any regulatory authority. 2 September 2019 Committed to Developing Life-changing Medicines Innovative Combinatorial Approaches Resourced for Success Nine immuno-oncology clinical candidates $272M Cash @ 06/30/19(a) Multiple alliances with Fc optimization platform to enhance antibodies’ immune activation leading biopharma companies Commercial scale GMP Leading bispecific DART® platform to exploit multiple mechanisms manufacturing facility ~380 Employees Multi-program “franchises” around high-value targets (B7-H3, PD-1) (Rockville, MD & SF Bay Area) (a) Includes cash equivalents and marketable securities. 3 September 2019 Broad Array of Engineered Antibody Formats Engaging the Immune System to Target Cancer Fc-Optimized Antibody Drug Antibody DART/TRIDENT™ Molecules Antibody Conjugate Bivalent Bivalent Bivalent Bivalent Tetravalent Trivalent Monospecific Monospecific Monospecific Bispecific Bispecific Trispecific Fab Region Fc Region Key Features: • Enhance Fc-mediated • Leverage 3rd party • “Plug-and-play” multi-specific platforms activity, incl. ADCC linker-payload tech • Tailored half-life and avidity/valency to optimize product profile • Promote innate and (Synthon, Immunogen) • Broad range of modalities pursued: adaptive immunity • Deliver potent anti- – Co-blockade of multiple checkpoint molecules • Combine with tumor payload – Redirect T-cell killing checkpoint inhibitors – to augment activity Tumor-directed co-stimulation 4 September 2019 Our Advancing Immuno-Oncology Pipeline Retains major market commercial rights for 8 of 9 development candidates Program (Target) Potential Indication Pre-IND Phase 1 Phase 2 Phase 3 Collaborator Our Commercial Rights Margetuximab (HER2) Breast (HER2+) “SOPHIA” Zai Lab, Worldwide, excluding South Korea GC Pharma and Greater China Gastric (+anti-PD-1) Enoblituzumab (B7-H3) Solid Tumors (+anti-PD-1) I-Mab Biopharma Worldwide, excluding Greater China H3 - MGD009 (B7-H3 × CD3) Solid Tumors (+MGA012) — Worldwide B7 MGC018 (B7-H3)(a) Solid Tumors — Worldwide MGA012 (PD-1) Solid Tumors Incyte(b) — 1 - MGD013 (PD-1 × LAG-3) Solid Tumors/Heme Mal. Zai Lab Worldwide, excluding Greater China PD MGD019 (PD-1 × CTLA-4) Solid Tumors — Worldwide Flotetuzumab (CD123 × CD3) AML — Worldwide AML (+MGA012) MGD007 (gpA33 × CD3) Colorectal (+MGA012) — Worldwide “MGD” = DART “MGA” = Antibody “MGC” = ADC (a) MGC018 is an antibody-drug conjugate (ADC) based on a duocarmycin payload with cleavable peptide linker that was licensed from Synthon Biopharmaceuticals. (b) MacroGenics retains rights to develop its pipeline assets in combination w/MGA012 (INCMGA0012) and to manufacture a portion of global clinical and commercial supply needs of MGA012. All Company product candidates described or mentioned herein are investigational and have not yet been approved for marketing by any regulatory authority. 5 September 2019 Core Product Candidates with Key Milestones Anticipated in 2019 Enhance Innate Margetuximab Enoblituzumab Immune Function (Anti-HER2 mAb) (Anti-B7-H3 mAb) through Fc Optimization (a) Restore and MGA012 MGD013 Flotetuzumab Redirect T-Cell (Anti-PD-1 mAb) (PD-1 × LAG-3 DART) (CD123 × CD3 DART) Function (a) MacroGenics retains rights to develop its pipeline assets in combination with MGA012 (INCMGA0012) and to manufacture a portion of global clinical and commercial supply needs of MGA012. 6 September 2019 Building Competitive Advantage Around Combinatorial Mechanisms Tumor Destruction Restore T-Cell Function: Enhance T-cell Function: and Antigen Presentation Checkpoint Inhibition T-Cell Recruitment Complementary MOA’s Complementary MOA’s MGA012 Flotetuzumab Margetuximab or Enoblituzumab MGD013 TAA: tumor-associated antigen 7 September 2019 Margetuximab Margetuximab: Anti-HER2 mAb Engineered to Enhance Activity of Immune System Positive results from pivotal phase 3 study presented at ASCO 2019 • Inhibits HER2 signaling (similar to trastuzumab) Function/ • MoA Fc region engineered to engage innate and adaptive immunity as mediators of anti-tumor activity HER2 HER2 • Ph. 3 SOPHIA study in HER2+ metastatic breast cancer Fab Pivotal Region Clinical • Ph. 2/3 MAHOGANY study w/checkpoint inhibitor in Studies HER2+ gastric cancer (anticipated start 3Q19) • Ph. 3 SOPHIA study ‒ Positive PFS results reported ASCO 2019 Fc Region Program ‒ Interim OS results expected 4Q19, final OS in 2020 Status • BLA submission in HER2+ mBC expected 4Q19 • Ph. 1 HER2+ gastric cancer data reported ASCO GI 2019 MacroGenics’ Retained • Global rights (excl. Greater China, South Korea) Rights Margetuximab is investigational and has not yet been approved for marketing by any regulatory authority 8 September 2019 Margetuximab 3rd/4th Line HER2+ Metastatic Breast Cancer Represents Attractive Entry Point mBC Line of Therapy 1st Line 2nd Line 3rd/4th Line Annual # of Patients(a) ~19,200 ~16,000 ~18,800 No consensus Trastuzumab T-DM1 (lapatinib + capecitabine; Standard of Care + pertuzumab (ado-trastuzumab trastuzumab + different + taxane (docetaxel) emtansine) chemo) Median OS 56.5 months(b) 30.9 months(c) 15.8 months(d) Median PFS 18.5 months(b) 9.6 months(c) 3.3 months(e) ORR 80.2%(b) 43.6%(c) 8.6% (a) US/EU5 Data from 9/13/18 Roche Virtual Late Stage Pipeline Event (b) Baselga, et al. – CLEOPATRA Study Group; Perjeta package insert (c) Verma, et al. – EMILIA Study Group; Kadcyla package insert (d) Krop, et al., The Lancet (June 2017) – TH3RESA Study Group (e) Krop, et al., The Lancet (May 2014) – TH3RESA Study Group 9 September 2019 Margetuximab Phase 3 Study Comparing Margetuximab to Trastuzumab SOPHIA clinical trial designed to support registration in 3rd/4th line HER2+ metastatic breast cancer Arm 1 margetuximab + HER2+ mBC Investigator’s Choice of chemotherapy 1–3 Prior Treatment Lines Chemotherapy in Metastatic Setting 1:1 Randomization (N = 536) (capecitabine, eribulin, R (including prior treatment with gemcitabine or vinorelbine) multiple other anti-HER2 agents)(a) Arm 2 trastuzumab + chemotherapy • Sequential primary endpoints: PFS and OS − PFS and first interim OS analyses as of October 2018 − Second interim OS analysis planned at 270 events in 2H2019 − Final OS analysis planned at 385 events in 2020 Global sites: ~200 • Patients carrying CD16A (FcγRIIIa) 158F allele were pre-specified PFS (N=257, HR=0.67, α=0.05, power=90%) exploratory subpopulation OS (N=385, HR=0.75, α=0.05, power=80%) (a) All study patients had previously received trastuzumab and pertuzumab, and approximately 90% had previously received ado-trastuzumab emtansine. 10 September 2019 Margetuximab SOPHIA Ph. 3 Demonstrated Superiority to Trastuzumab in Primary PFS Endpoint PFS prolonged in margetuximab arm vs. trastuzumab arm PFS Primary Endpoint (ITT Population):